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Your Child

263,000 iPhone Cases Recalled Due to Burn and Skin Irritations

1:30

About 263,000 MixBin Electronics iPhone cases are being recalled because liquid and glitter can leak out of the cases, causing skin irritation and burns to consumers.

This recall involves all liquid glitter mobile phone cases for iPhone 6, 6s and 7. The cases contain liquid and glitter that are floating in the plastic case. They were sold in various styles and colors and measure about 5.5 inches by 2.75 inches. The model number and UPC can be found on the product's packaging. To view model numbers, UPC codes and photos, please visit: https://www.cpsc.gov/Recalls/2017/MixBin-Electronics-Recalls-iPhone-Cases/

There have been 24 reports worldwide of skin irritation or chemical burns, including 19 in the U.S. One consumer reported permanent scarring from a chemical burn and another consumer reported chemical burns and swelling to her leg, face, neck, chest, upper body and hands. 

The iPhone cases were sold on Amazon and at Henri Bendel, MixBin, Nordstrom Rack, Tory Burch and Victoria's Secret stores nationwide and online from October 2015 through June 2017 for between $15 and $65.

Consumers should immediately stop using the recalled cases and contact MixBin Electronics for a full refund.

Consumers can contact MixBin Electronics toll-free at 855-215-4935 from 8 a.m. to 5 p.m. ET Monday through Friday, or online at www.getmixbin.com for more information. 

This recall was conducted voluntarily by the company under CPSC's Fast Track Recall process. Fast Track recalls are initiated by firms who commit to work with CPSC to quickly announce the recall and remedy to protect consumers.

Story source: http://www.prnewswire.com/news-releases/mixbin-electronics-recalls-iphone-cases-due-to-risk-of-skin-irritation-and-burns-300497584.html

Your Baby

Recall: Otteroo Baby Floats Due to Drowning Risks

1:00

Babies and young children can drown in less than 2 inches of water.  That’s why it is  vital that parents and caregivers never leave a baby or young child unattended while they are near or in water.

When bathing their infant, parents will sometimes attach a bath float to their child to help keep his or her head above water. While the float may offer some assistance, critics warn that the device can give parents a false sense of security that their child is protected from drowning.

Otteroo Corporation makes inflatable baby floats that are specifically designed for babies 8 weeks and up.

The company is recalling about 3000 units of their inflatable Baby Floats after receiving 54 reports of broken seems on the product. No injuries have been reported.

The Otteroo Inflatable Baby Float is an inflatable round ring made of clear and blue plastic material. It has two air chambers that fasten around a baby’s neck with a white buckle. The floats have a chin rest, two handles and two circular openings on the back of the ring to allow the device to expand as the child grows with age. There are three colorful balls that move freely around inside the ring.  The name “Otteroo” is imprinted on the top of the float in large, orange letters with an Otter logo.

Consumers should immediately stop using the recalled inflatable baby floats and contact the firm to receive a free replacement.

The floats were sold online at Otteroo.com and Amazon.com and Zulily.com from January 2014 through July 2014 for about $35.

Consumers can contact Otteroo Corporation at (415) 236-5388 from 9 a.m. to 5 p.m. PT Monday through Friday or online www.otteroo.com and click on “Safety” at the bottom of the page for more information.

According to their website, Otteroo is offering a free replacement for those who purchased the product manufactured in 2014 (NO: 002013001).

Sources: http://www.cpsc.gov/en/Recalls/Recall-Alerts/2015/Otteroo-Corp-Recalls-Inflatable-Baby-Floats/

http://otteroo.com/pages/safety-info

Parenting

Recall: Samsung Washing Machine –Top Can Detach

1:30

Washing machines are a necessity for growing families. If you own a Samsung top-loading washer, family members could be in danger of being injured if the top detaches during use.

About 2.8 million Samsung top-loading washing machines are being recalled after 733 reports of the washing machines experiencing excessive vibration or the top detaching from the washing machine chassis.  There are nine related reports of injuries, including a broken jaw, injured shoulder, and other impact or fall-related injuries.

This recall involves 34 models of Samsung top-load washing machines.  The washing machines have mid-controls or rear-controls. Model numbers and serial information can be found on two labels affixed to the back of the machine.. Consumers should check with Samsung to see if their washer is recalled.

A list of the models affected by this recall can be found online at www.Samsung.com and click on the recall notice at the top of the page for more information. You can also call 866-264-5636 from 8 a.m. to 10:00 p.m. Eastern Standard Time.

If you own one of the recalled models, contact Samsung immediately to receive one of the following remedy options. Consumers can choose (1) a free in-home repair that includes reinforcement of the washer’s top and a free one-year extension of the manufacturer’s warranty; (2) a rebate to be applied towards the purchase of a new Samsung or other brand washing machine, along with free installation of the new unit and removal of old unit; or (3) a full refund for consumers who purchased their washing machine within the past 30 days of the recall announcement.

All known consumers will also receive a Home Label Kit that includes a control panel guide and additional safety instructions in the mail.

Until they have received and installed a Home Label Kit, consumers should only use the delicate or waterproof cycles when washing bedding, water-resistant and bulky items.  The lower spin speed in the delicate or waterproof cycles lessens the risk of the washing machine top unexpectedly detaching from the washing machine chassis.

The washing machines were sold at Best Buy, The Home Depot, Lowes, Sears and other home appliance stores nationwide from March 2011 to November 2016 for between $450 and $1,500.

Story source: https://www.cpsc.gov/Recalls/2017/Samsung-Recalls-Top-Load-Washing-Machines

  

 

 

Your Toddler

Safety 1st Recalls Décor Wood Highchairs Due to Falls

1:30

Dorel Juvenile Group, of Columbus, Ind., is recalling about 35,000 Safety 1st Wood Décor highchairs because a child can remove the highchair’s tray, posing a fall hazard.

Safety 1st has received 68 reports of children removing the trays and 11 reports of injuries such as lacerations, chipped teeth and bruises.

The highchairs were sold at Babies R US and Toys R Us retail stores nationwide and online at www.Amazon.com, www.BabiesRUs.com, www.ToysRUs.com and www.Walmart.com and other online retailers from May 2013 through May 2015 for about $120.

This recall includes Safety 1st Wood Décor highchairs in three models: HC144BZF (Casablanca), HC229CZF (Gentle Lace) and HC229CYG (Black Lace). The model numbers are printed under the highchair seat. These A-frame black wood highchairs have a removable fabric, black and white print seat pad with a blue or pink border on the top and bottom of the seat pad. The highchairs have a white plastic, detachable tray with a cone-shaped center divider that fits between a child’s legs. “Safety 1st” is printed on the front center of the tray.

Consumers should immediately stop using these recalled highchairs and contact the firm to receive instructions on receiving a new tray with labels.   

Consumers can contact Safety 1st toll-free at (877) 717-7823 from 8 a.m. to 5 p.m. ET Monday through Friday, email at decorwoodhighchair@djgusa.com or online at www.safety1st.com and click on “Safety Notices” at the top of the page for more information.

Source: http://www.cpsc.gov/en/Recalls/2016/Safety-1st-Recalls-Decor-Wood-Highchair/

 

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!

Your Child

Recall: CLIF Bars, Due to Possible Nut Allergens

2:00

If your child has a nut allergy, and eats CLIF bars, they could accidently ingest one of an assortment of nuts that may have slipped through the manufacturing process.

CLIF Bar and Company is voluntarily recalling 12 of its products that are primarily marketed for children because they may contain several nut allergens.

The bars might contain peanuts, walnuts, almonds, hazelnuts, cashews, Brazil nuts, macadamia nuts, pecans and coconut.

As you know, serious or life-threatening allergic reactions are possible for those with severe allergy to nuts or peanuts. As this time, there have been no reports of illness from this recall.

The bars were sold online and at retail stores throughout the United States. The affected products can be identified by the “Best By” date code found on the back of the individual packaging. You can check the lot codes below:

  • CLIF BUILDER'S 18-count Variety Pack Chocolate Peanut Butter and Chocolate Mint: Lot Code FROM: 24MAR16M; Lot Code TO: 08FEB18M
  • CLIF Kid Zbar Protein 30-count Variety Pack -- Lot Code FROM: 31MAY16M; Lot Code TO: 15OCT17M
  • CLIF BUILDER'S Chocolate Mint 12-count -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3
  • CLIF BUILDER'S Chocolate Mint 6-pack -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF BUILDER'S Chocolate Mint 7-pack -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF BUILDER'S Snack Size Chocolate Mint 200-count -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF Kid Zbar Protein Chocolate Chip 10-pack -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF Kid Zbar Protein Chocolate Chip 150-count -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF Kid Zbar Protein Chocolate Chip 5-pack -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF Kid Zbar Protein Chocolate Mint 10-pack -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF Kid Zbar Protein Chocolate Mint 150-count -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 
  • CLIF Kid Zbar Protein Chocolate Mint 5-pack -- Lot Code FROM: 05APR16M3; Lot Code TO: 23APR18M3 

All other CLIF Bar and Company products are not affected by this recall.

The company is asking people to return the products to where they bought them for a refund or exchange. People with questions can call 866-526-1970 or visit the company’s website here.

Story source: Brunilda Nazario, MD http://www.webmd.com/diet/news/20170706/clif-bars-recall

http://www.clifbar.com/text/june-2017-recall

Your Baby

49,000 Britax B-Ready Baby Strollers Recalled

1:45

About 49,000 Britax B-Ready strollers have been recalled because the foam padding on the stroller’s arm bar can come off in fragments if the child bites the arm bar, posing a choking hazard.

This recall involves Britax B-Ready strollers and B-Ready replacement top seats that were sold separately. The B-Ready strollers have a silver or black frame with a solid-colored top seat in a variety of colors. The Britax logo is on the stroller’s side hinges and foot rest. B-Ready is printed on the sides of the stroller frame.  The stroller’s model number and date of manufacture are printed on a label on the stroller’s frame between the front wheels or on the inside frame that connects to the back right wheel. The replacement top seats were sold separately in a variety of colors and fit into the stroller’s frame. The replacement top seat’s model number and date of manufacture are printed on a black label on the right side tube above the adjuster button, under the fabric cover.

Britax has received 117 reports of children biting the arm bar foam padding, including five reports of children choking or gagging on foam fragments.

Consumers should immediately remove the arm bar from recalled strollers and replacement top seats and contact Britax for a free black, zippered arm bar cover and a warning label to apply to the strollers and replacement top seats. Consumers can continue to use their strollers without the arm bar attached.

The strollers were sold at Babies R Us, buybuy Baby, Target and other stores nationwide and online at Amazon.com, Diapers.com and other websites from April 2010 through January 2016 for about $500 for the stroller. Britax sold the replacement top seats from April 2010 through January 2016 for about $150.

The model numbers for the B-Ready Strollers are:

U281767, U281768, U281771, U281772, U281773, U281774, U281784, U281792, U281793, U281794, U281795, U281796, U281797.

The B-Ready replacement top seats model numbers are:

S845600, S845700, S845800, S845900, S855000, S855100, S856600, S870200, S870300, S870600

These models were sold April 1, 2010 (2010/04/01) through Dec. 31, 2012 (2012/12/31).

 Consumers can contact Britax at 800-683-2045 from 8:30 a.m. to 5:45 p.m. ET Monday through Thursday and from 8:30 a.m. to 4:45 p.m. ET on Friday, by email at Britax.Recall@britax.com or online at www.us.britax.com and click on Safety Notice at the top right, or  www.B-ReadyRecall.com for more information.

Source: http://www.cpsc.gov/en/Recalls/2016/Britax-Recalls-Strollers-and-Replacement-Top-Seats/

Your Baby

Recall: Infant Bathtubs Due to Drowning and Impact Injury

1:30

This recall involves 86,000 Summer Infant Lil’ Luxuries Whirlpool, Bubbling Spa & Shower with fabric slings.

Fabric slings on the recalled infant bathtubs can detach from the tub, posing a risk of impact injury and drowning.

CPSC and Summer Infant have received reports of 91 incidents of the sling detaching, including 11 reports of infants who received a bump to the head.

The infant bathtub is a battery-operated whirlpool bath with motorized jets intended for use with children from birth to 2 years. The product contains a fabric sling on a plastic frame onto which the infant is placed for bathing. The fabric sling on the recalled bathtubs does not have a white plastic attachment clip to hold the headrest area of the fabric sling to the plastic frame.

Recalled bathtubs have item numbers 18840, 18850, 18863, and 18873 and were sold between October 2012 and October 2013 with date codes starting with 1210, 1211, 1212, 1301, 1302, 1303, 1304, 1305, 1306, 1307, and 1308, which stand for the two-digit year followed by the two-digit month, on the fabric sling.

Consumers should immediately stop using the fabric sling in the recalled product and contact Summer Infant for a replacement fabric sling with a white plastic attachment clip. Consumers can contact Summer Infant toll free at 844-612-4254 from 9 a.m. to 5 p.m. ET Monday through Thursday and 9 a.m. to 3 p.m. ET on Friday, or online at www.summerinfant.com and click on “Safety Alerts & Recalls” at the bottom of the page for more information.

The recalled items 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. CPSC and Summer Infant warn consumers that these tubs could have been and could continue to be sold on the secondhand market.

 

Your Baby

IKEA Recalls 169,000 Crib Mattresses

1:30

Swedish furniture maker IKEA is recalling about 169,000 of their VYSSA crib mattress because of the risk that infants can become trapped between the mattress and the crib.

The firm has received two reports of infants becoming entrapped between the mattress and an end of the crib. The children were removed from the gap without injury.

The mattresses were sold exclusively at IKEA stores and online from August 2010 to May 2014 for about $100.00.

This recall involves IKEA VYSSA style crib mattresses with the following five model names:

·      VACKERT

·      VINKA

·      SPELEVINK

·      SLÖA

·      SLUMMER.

The involved mattresses were manufactured on May 4, 2014 or earlier. An identification label attached to the mattress cover has the date of manufacture in Month-DD-YYYY format and the VYSSA model name. A gap between the mattress and crib ends larger than two-finger width is an indication of the defective mattress.

Consumers should inspect the recalled mattress by making sure there is no gap larger than the width of two fingers between the ends of the crib and the mattress. If any gap is larger, customers should immediately stop using the recalled mattresses and return it to any IKEA store for an exchange or a full refund.

Consumers can contact IKEA toll-free at (888) 966-4532 anytime or online at www.ikea-usa.com and click on the recall link at the top of the page for more information.

Source: http://www.cpsc.gov/en/Recalls/2015/IKEA-Recalls-Crib-Mattresses/

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