Twitter Facebook RSS Feed Print
Your Child

Safety Recalls: Finger Paints, Baby Bathtubs, Strollers and More

2:00

The American Academy of Pediatrics’ (AAP) online Gateway issue has listed several children’s products that have been recalled due to health and safety concerns.

The list includes

·      Sargent Art tempera finger paints, Lil’ Luxuries Whirlpool, Bubbling Spa & Shower

·      Peg Perego’s 850 Polaris Sportsman ATV-style ride on toy

·      Mamas & Papas’ Armadillo Flip and Armadillo Flip XT strollers

·      Fiddle Diddles LullaBelay adjustable car seat strap system

·      Chimparoo brand Trek baby carriers

Sargent Art tempera finger paints: About 2.8 million units of paint have been recalled. The paint can contain harmful bacteria, putting children with weak immune systems at risk of serious illness. Those with healthy immune systems may not be affected.

Recalled are 13 types of Sargent Art tempera and finger paints. All colors and sizes of the following types of paints are recalled: Art-Time brand of tempera paint, washable finger paint, washable fluorescent finger paint, washable fluorescent tempera paint, washable glitter finger paint, washable paint and fluorescent tempera paint.

Sold at: Hobby Lobby, Wal-Mart and other stores nationwide and online at Amazon.com and ShopSargentArt.com from May 2015 to June 2016 for $1 to $8.

Stop using the paints and contact the company for a refund at 800-827-8081 or visit www.sargentart.com.

Lil’ Luxuries Whirlpool, Bubbling Spa & Shower: About 86,000 units have been recalled. Fabric slings can come off the infant bathtubs, and infants can fall or drown.

Lil’ Luxuries Whirlpool, Bubbling Spa & Shower is a battery-operated whirlpool bath with motorized jets intended for use with children from birth to 2 years. The product has a fabric sling on a plastic frame onto which the infant is placed for bathing. The fabric sling on the tub does not have a white plastic clip to attach the headrest area of the fabric sling to the plastic frame. Recalled bathtubs have numbers 18840, 18850, 18863 or 18873 with date codes starting with 1210, 1211, 1212, 1301, 1302, 1303, 1304, 1305, 1306, 1307 or 1308, which stand for the two-digit year followed by the two-digit month, on the fabric sling.

The products were sold at Toys R Us/Babies R Us and other juvenile product specialty stores nationwide from October 2012 through October 2013 for about $60. The tubs also might have been sold secondhand.

Stop using the fabric sling in the tub, and contact the company for a replacement sling with a white plastic attachment clip. You can call 844-612-4254 or visit http://bit.ly/2f1wQNG.

Peg Perego’s 850 Polaris Sportsman ATV-style ride on toy, About 3,000 toys were recalled. A relay on the circuit board can fail causing the vehicle’s motor to overheat and catch fire.

Recalled are Peg Perego’s 850 Polaris Sportsman ride-on, 24-volt battery-operated toy vehicles for children ages 5 to 7 years. The ATV-style vehicles for two people are silver, red and black and have four wheels, a flip-up backrest for the back passenger and a front and rear luggage rack. Vehicles with date codes 651016, 651017, 651020, 651021, 651022, 651023, 651024, 651027, 651028, 651029, 651030, 660304, 660305, 661123, 661124, 661125 and 661130 are recalled. The date code is under the vehicle seat. Sportsman Twin and 850 EFI are printed on the side and Polaris is on the side of the seat.

Items were sold at online retailers including Amazon.com, Cabelas.com, Target.com, ToysRUs.com and Walmart.com from October 2014 through April 2016 for $500 to $600.

Remedy is to Contact Peg Perego for a replacement circuit board with instructions, including shipping. Call 877-737-3464, email 850recall@pegperego.com or visit https://us.pegperego.com/cs/recalls/.

Mamas & Papas’ Armadillo Flip and Armadillo Flip XT strollers: About 3,000 strollers have been recalled. A loose latch on the stroller can cause the infant in the seat to tip back unexpectedly and possibly fall out when facing the parent.

Recalled are Mamas & Papas’ Armadillo Flip and Armadillo Flip XT strollers. All models are folding strollers for one infant. They come in black, teal and navy and weigh about 22 pounds. Lot number ranges for recalled Armadillo Flip strollers are 00814 through 00416. Lot number ranges for the Flip XT are 01214 through 00416. The number is printed on the sewn-in label on the stroller.

Strollers were sold at Albee Baby, Babies ‘R’ Us, Buy Buy Baby and other stores nationwide and online at www.mamasandpapas.com and www.amazon.com from December 2014 through July 2016 for $500.

Stop using the strollers and contact the company for a repair at 800-309-6312 or visit www.mamasandpapas.com/us.

Fiddle Diddles LullaBelay adjustable car seat strap system: About 250 units have been recalled. The carabiners attached to the strap system have small parts inside that can come loose and be swallowed and choked on by young children.

The Fiddle Diddles LullaBelay adjustable car seat strap system with model number LB1001 includes two fabric straps, carabiner hardware, a mesh car seat cover and a tote bag. The carabiners are used to hang a car seat from a shopping cart. The model number is printed on the straps.

They were sold at Amazon.com from November 2015 through June 2016 and Fiddlediddles.com from May through June 2015 and at Zoolikins stores in Arizona from November 2015 through June 2016 for about $40.

You can contact the company for a repair kit with three new carabiners. Call 888-741-2957, email info@fiddlediddles.com or visit http://fiddlediddles.com/replacement-kit.html.

Chimparoo brand Trek baby carriers: About 130 units are being recalled. The carriers’ side strap can loosen unexpectedly from the buckle, and the child can fall out.

Recalled are Chimparoo brand Trek baby carriers that allow the user to carry a baby tummy to tummy, on the hip or on the back. The 100% twill fabric carriers were sold in 18 solid, striped and pattern color combinations. The carriers attach to the wearer’s body with adjustable straps made of polypropylene webbing and plastic buckles. “Chimparoo” is printed on the upper right hand corner of the carrier. “Trek” is embroidered on the belt.

The carriers were sold at Children’s boutique stores, such as Granola Babies, of Costa Mesa, Calif., Eat/Sleep/Play, of Summerville, S.C., and Top to Bottom, of Omaha, Neb., and online at www.Amazon.com and www.Chimaparoo.ca from May through July 2016 for about $170.

Contact the company for a replacement buckle for the baby carrier’s side-buckle. Call 855-289-5343, email safety@Chimparoo.com or visit www.Chimparoo.ca/en/recall.

Story source: Trisha Korioth, at http://www.aappublications.org/news/2016/11/17/HealthAlerts111716

Your Baby

Beech-Nut Recalls Baby Food Due to Pieces of Glass

1:00

The Beech-Nut Nutrition Company has issued a voluntary recall of 1,920 pounds of baby food due to possible contamination with small pieces of glass.

The company is recalling “Stage 2 Beech-Nut Classics sweet potato and chicken” baby food in 4 -ounce glass jars.  The baby food was made on Dec. 12, 2014, and the recall applies to food expiring December 2016.

A customer reported that they found a small piece of glass in their baby food and the United States Department of Agriculture (USDA) says that an oral injury, from use of the product, was also conveyed.

“Outside of this single report, we have no indication that any other jar of our Classics Stage 2 Sweet Potato & Chicken is affected, but as a company of parents and families we are acting with an abundance of caution,” the company said in a statement posted to its website. “The quality and safety of our products is our number one priority. We know we have not met the expectations of parents who rely on Beech-Nut for quality nutrition for their babies and toddlers in this case, and for that we apologize.”

The recalled baby food contains the product numbers “12395750815” through “12395750821.” It also contains the inspection code “P-68A.”

Consumers who have purchased the baby food can return it to the store where it was purchased for a refund. You can also call Beech-Nut at (866) 674-4446 with any concerns or for a full refund.

More recall information is located on the Beech-Nut website at  http://www.beechnut.com/recall.

Consumers should not use the product and if you suspect your baby has eaten the baby-food, Beech-Nut recommends parents should consult with their pediatrician or family physician. 

Your Baby

Alert! 180,000 Baby Pacifiers Recalled Due to Choking Hazard

1:30

Munchkin is recalling their Lightweight Pacifiers and Clips. The clip cover can detach from the pacifier’s clip, posing a choking hazard for young children.

his recall involves Munchkin’s Latch lightweight pacifiers and clips sold as a set. The pacifiers were sold in five styles: designer, rattle and heartbeat clips with 0m+ natural shape pacifiers, and designer and rattle clips with 6m+ orthodontic pacifiers. The designer pacifiers and clips 0m+ and 6m+ are in three color patterns: blue and white strips, orange and with white polka dots and pink with white polka dots. The rattle pacifiers and clips 0m+ and 6m+ are green with beads in the pacifier cover to make a rattle sound and have a polka dot strap. The heartbeat pacifiers and clips have a red, heart-shaped pacifier cover and red and white polka dots on the strap.

About 180,000 of the pacifier and clip sets have been sold. They were available from Babies R Us, Target, Wal-Mart and other mass merchandisers, juvenile product, baby boutique and discount stores nationwide and online at amazon.com, munchkin.com and other website from March 2014 through March 2016 for between $11 and $15.

The firm has received 10 reports (5 in the U.S. and 5 in Canada) of the clip cover detaching from the pacifier clip. No injuries have been reported. 

Consumers should immediately take the clip away from young children and contact Munchkin for a free replacement Lightweight Pacifier pack with two pacifiers or a full refund.

There is a toll-free consumer hotline available for more information at 877-242-3134 from 7 a.m. to 5 p.m. PT Monday through Friday or online at www.munchkin.com, click on Help at the bottom of the page and then Recalls for more information.

Story source: http://www.cpsc.gov/en/Recalls/2016/Munchkin-Recalls-Latch-Lightweight-P...

Your Baby

Safety Recall: Infant Bicycle Helmets

1:30

Pacific Cycle is recalling about 129,000 bicycle helmets with magnetic no-pinch buckle chinstraps, due to choking and magnet ingestion hazards. These helmets are sold exclusively at Target stores.

The magnetic buckle on the helmet’s chinstrap contains small plastic covers and magnets that can come loose, posing a risk of choking and magnet ingestion to young children.

The helmets are made for infants ranging from one to three years old. The helmet and its straps come in various colors and design patterns. The buckles have small plastic covers and enclosed magnets. “SCHWINN” is printed on the front of the helmets. Only helmets with the magnetic no-pinch chinstrap buckles are affected by this recall.

Pacific Cycle has received three reports of the plastic cover coming loose. No injuries have been reported.

Consumers should immediately take the helmets away from children and contact Pacific Cycle for instructions on how to receive a free replacement helmet.

The helmets were sold exclusively at Target stores and online at www.target.com from January 2014 through April 2016 for between $18 and $25.

Consumers can contact Pacific Cycle toll-free at 877-564-2261 from 8 a.m. to 5 p.m. CST Monday through Friday, email customerservice@pacific-cycle.com or online at www.schwinnbikes.com and click on “Support” then “Safety & Recalls” or www.target.com and click on “Product Recall” for more information. 

Source: http://www.cpsc.gov/en/Recalls/2016/Pacific-Cycle-Recalls-Infant-Bicycle-Helmets/

Your Toddler

Recall: Strollers and Rumble Seats Due to Choking Hazards

1:45

UPPAbaby is recalling about 71,000 of its’ 2015 CRUZ, 2015 VISTA strollers and 2015 RumbleSeat. The strollers’ and RumbleSeats’ bumper bar poses a choking hazard when a child bites the bumper bar and removes a piece of the foam covering.

UPPAbaby has received 22 reports of children biting off a piece of the bumper bar foam. No injuries have been reported.

The strollers and rumble seats were sold at BuyBuy Baby and other juvenile product retailers nationwide and online at Amazon.com from December 2014 through July 2015 for about $500 for the CRUZ stroller, $860 for the VISTA stroller and $170 for the RumbleSeat.

Consumers should immediately remove and stop using the bumper bar on these recalled strollers and RumbleSeats and contact the firm to receive a free bumper bar cover and warning label.

The CRUZ strollers have an aluminum alloy grey or black frame with a black fabric toddler seat with a colored fabric sunshade canopy and a black basket under the seat. The UPPAbaby name and logo are printed on the side of the canopy and “CRUZ” is printed in white lettering on the handlebars of the stroller.

The VISTA strollers have grey or black aluminum frames, colored sunshade canopy and are made to hold one, two or up to three children. VISTA is printed in white lettering on the handlebars of the stroller and UPPAbaby is printed across the bottom diagonal rail of the stroller frame next to a black, fabric basket.

The RumbleSeat is a separate seat attachment that can be attached to the stroller frame. RumbleSeats have manufacture dates stamped on the bottom of the seat from September 2014 through May 2015. The RumbleSeat comes in various colors and allows the child to ride rear facing, forward facing or reclined.

All of the strollers and RumbleSeats have a foam bumper bar across the middle of the product for the child to hold.

The recalled stroller and rumble seat model numbers are listed online at http://www.cpsc.gov/en/Recalls/2015/UPPAbaby-Recalls-Strollers-and-RumbleSeats/#remedy.

Consumers can also contact UPPAbaby customer service toll-free at (844) 540-8694 from 9 a.m. to 5 p.m. ET Monday through Friday, email contact@uppababy.com or online at www.UPPAbaby.com and click on Safety Notice on the lower right hand corner of the page for more information.

Your Baby

Recall: Tommee Tippee Electric Bottle and Food Warmers Due to Fire Hazard

1:30

Mayborn USA is recalling about 255,000 Tommee Tippee electric bottle and food warmers because they could overheat and catch fire, according to the U.S. Consumer Product Safety Commission.

This recall involves Tommee Tippee® Closer to Nature® electric bottle and food warmers, sold separately or as an accessory with the Complete Starter Kit or the All in One Newborn Set. The bottle and food warmer is white with a gray adjustable control dial located next to the on/off light. Tommee Tippee is stamped in gray on the front of the unit. It measures about 5 inches high, 5 ½ inches wide and 5 inches long. Bottle and food warmers included on this recall have “Min” or “0” stamped on the left-hand side of the control dial and have the UL logo and a six alpha-numeric batch code that begins with a number and ends with “GY” stamped on the underside. Consumers should visit www.tommeetippee.us/bottle-warmer to complete the free replacement registration form.

The firm has received six reports of bottle and food warmers overheating, melting, smoking and catching on fire; which resulted in $16,000 in property damage.

Consumers should immediately unplug and stop using the recalled bottle and food warmers and contact Mayborn for free replacement warmers.  

The product was sold at merchandise stores including Baby Depot, Baby Heaven, Bealls Outlet, BuyBuy Baby, CVS, Giant, Ideal Baby and Kids, Kohl’s, Marco Baby, Marshalls, Meijer, Ross Stores, Sam’s Club, Target, TJ Maxx, Toys R Us, Walgreens and Wal-Mart nationwide and online at Amazon.com, Diapers.com, Drugstore.com and Quidsi.com from July 2011 through April 2016 for about $21 for the individual bottle and food warmer and about $120 for the starter kit or newborn set.

Consumers can contact Mayborn online at www.tommeetippee.us and click on the recall button at the bottom of home page or toll-free at 844-340-3420 from 9 a.m. to 5 p.m. ET Monday through Saturday for more information.

This Mayborn recall follows another recent recall from the company. In May 2016, over 3 million Tommee Tippee Sippee Spill-Proof Cups were recalled due to the possibility of mold build-up in the removable, one-piece white valve.

Mayborn USA had received 3,066 reports of mold in the removable, one-piece, opaque valve of the Sippee cups, including 68 reports of children experiencing diarrhea, vomiting or other symptoms associated with drinking from a cup with mold in the valve.

Story sources: https://www.cpsc.gov/en/Recalls/2016/Tommee-Tippee-Electric-Bottle-and-Food-Warmers-Recalled-by-Mayborn-USA/

http://www.cpsc.gov/en/Recalls/2016/Tommee-Tippee-Sippee-Cups-Recalled-by-Mayborn-USA/

Your Child

Recall: More Than 590,000 Albuterol Inhalers

1:30

Adults and children with breathing problems often rely on metered dose inhalers to open their airways, allowing them to breathe more easily. Albuterol (Proventil, Proair, Ventolin) is a medication called a bronchodilator, commonly found in rescue inhalers for acute asthma attacks.

GlaxoSmithKline is recalling more than 590,000 albuterol inhalers. Three lots of Ventolin HFA 200D inhalers have been voluntarily recalled due to a potential issue with the delivery system, a spokesman for the British pharmaceutical company said.

The affected lot numbers are 6ZP0003, 6ZP9944 and 6ZP9848. The devices have been recalled from hospitals, pharmacies, retailers and wholesalers in the United States.

The recalled inhalers may not release the correct dose of medication due to a defective delivery system. Albuterol opens airways in the lungs to treat common conditions such as asthma and chronic obstructive pulmonary disease.

The company said it had received an elevated number of product complaints about a bulging of the outside wrapper, indicating a leak of the propellant that delivers the medicine.

The U.S. Food and Drug Administration has approved the voluntary "Level 2" recall, which only affects products in the United States, GSK spokesman Juan Carlos Molina said.

The defect does not pose a danger to patients, so they are not being asked to return inhalers they have already purchased. However, if the devices are not relieving symptoms, patients should seek medical attention right away.

GSK said it was trying to identify the root cause of the problem and would take corrective action. Patients whose inhalers are among the affected lots can contact GSK’s customer service center at 1-888-825-5249.

Story sources: Robert Jimison, http://www.cnn.com/2017/04/06/health/albuterol-inhaler-recall/

Your Child

McDonald’s Recalls Kid's “Step-iT” Wristbands Due to Burns, Skin Irritations

1:30

About 29 million of McDonald’s “Step-iT” activity wristbands have been recalled in the U.S. due to skin irritations or burns to children.

The recall involves “Step-iT” activity wristbands, which come in two styles—“Activity Counter” and a motion-activated “Light-up Band.” The Activity Counter comes in translucent plastic orange, blue or green and features a digital screen that tracks a child’s steps or other movement. The Light-up Band comes in translucent plastic red, purple, or orange and blinks light with the child’s movement. Both styles of activity wristbands have a square face with the words “STEP-iT” printed on them and a button to depress and activate the wristband. The back of the square face contains the etched words “Made for McDonald’s.” 

The company has received more than 70 reports of incidents, including seven reports of blisters, after wearing the wristbands.

Consumers should immediately take the recalled wristbands from children and return them to any McDonald’s for a free replacement toy and either a yogurt tube or bag of apple slices.

The wristbands were distributed exclusively by McDonald’s restaurants nationwide, from August 9, 2016 to August 17, 2016 with Happy Meals and Mighty Kids Meals. 

Consumers can contact McDonald’s at 800-244-6227 from 7 a.m. to 7 p.m. CT daily, or online at www.mcdonalds.com and click on “Safety Recall” for more information. 

You can see all the models recalled on http://www.cpsc.gov/en/Recalls/2016/McDonalds-Recalls-Step-iT-Activity-Wristbands/

Daily Dose

Rotarix Vaccine Temporarily Suspended

The FDA suspends Glaxo Rotarix vaccine I received the CDC Health Alert yesterday afternoon notifying physicians to “temporarily suspend the usage of GlaxoSmithKline (GSK) Rotarix (rotavirus) vaccine. Rotarix was licensed for use in 2008 to prevent rotavirus disease, which typically causes fever, vomiting and diarrhea in infants and young children.

Prior to this Merck’s vaccine RotaTeq had been licensed for us in 2006. Both of these vaccines are given orally. Both RotaTeq and Rotarix were found to prevent serious rotavirus illness and hospitalizations for dehydration. The GSK product, Rotarix, which is a “live attenuated” vaccine, has been found to contain DNA from porcine circovirus type 1 (PCV 1). PCV 1 virus is not known to multiply in human cells or to cause illness.  According to the FDA, “all available evidence indicates that there had been no increased risk to patients who have received this vaccine”.  The GSK vaccine, Rotarix, is made in a different manner than the Merck vaccine RotaTeq.  Preliminary studies by the FDA on RotaTeq vaccine have not shown the presence of PCV 1 DNA. Preliminary data reported to the FDA  by GSK related to PCV 1 being in the vaccine seems to suggest that it has been present since the early stages of the vaccine’s development.  Studies on Rotarix, both before and after the approval of the vaccine, have shown it to be extremely safe and no unusual adverse events have been reported.  At the same time, the vaccines that have been given are presumed to be effective. In the interim, while futher studies are being completed, it is recommended that children continue to receive RotaTeq vaccine.  The FDA plans to convene an advisory committee to look into how the DNA components came to be present in this vaccine. They are also going to look into the use of new techniques for identifying viruses in vaccines.  After this meeting, the FDA will make further recommendations about the use of rotavirus vaccines in the United States. This recall was limited to the United States, and children in other areas or the world are continuing to receive Rotarix, as the available evidence suggests that the benefits of the vaccine outweigh the risks, especially in areas where rotavirus disease causes severe disease and even deaths. I would not be alarmed if my baby had received this vaccine as it does not cause disease in animals or humans.  I would also complete my child’s vaccine series with the Merck product which is available.  We will all have to stay tuned for further details,  but this should also make parents aware that the safety of vaccines continues to be monitored, even after they have been approved. That's your daily dose for today.  We'll chat again tomorrow! Send Dr. Sue your question now!

Pages

Please fill in your e-mail address to be included in our newsletter.
You may opt out at any time.

 

DR SUE'S DAILY DOSE

Does your child have trouble going to the bathroom?

Please fill in your e-mail address to be included in our newsletter.
You may opt out at any time.

 

Please fill in your e-mail address to be included in our newsletter.
You may opt out at any time.