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Your Toddler

Recall Reminder: 8th Child Dies From Fallen IKEA Dresser

2:00

IKEA has voluntarily issued a reminder about its recall of MALM and other models of chests and dressers due to a serious tip-over hazard. An 8th child has reportedly died after being trapped under a fallen IKEA dresser.

CEO Lars Petersson said Ikea wants to increase awareness of the recall campaign for several types of chest and dressers that can easily tip over if not properly anchored to a wall.

The initial recall was issued in June 2016, for 17.3 million chests and drawers. The Swedish retailer and the federal safety regulators are reminding customers to take immediate action to secure the dressers, or to return them.

This recall re-announcement involves MALM and other IKEA chests and dressers that do not comply with the requirements of the U.S. voluntary industry standard (ASTM F2057-14).  The recalled children’s and adult chests and dressers include the MALM 3-drawer, 4-drawer, 5-drawer and three 6-drawer models and other non-MALM models.  The recalled children’s chests and dressers are taller than 23.5 inches; recalled adult chests and dressers are taller than 29.5 inches. 

The MALM chests and dressers are constructed of particleboard or fiberboard and are white, birch (veneer), medium brown, black-brown, white stained oak (veneer), oak (veneer), pink, turquoise, grey, grey-turquoise, lilac, green, brown stained ash (veneer), and black.  A 5-digit supplier number, 4-digit date stamp, IKEA logo, country of origin and “MALM” are printed on the underside of the top panel or inside the side panel.  

To see a complete list of other non-MALM chests and dressers included in this recall, click on this link www.IKEA-USA.com or http://www.ikea.com/ms/en_US/ikea-chest-and-dresser-recall/index.htmlon IKEA’s website.

Dangerous tip-over incidents often occur when curious kids climb on furniture in an attempt to access TVs, toys, remotes or other desired items.  While the threat is serious, the solution is simple. Anchor TVs, furniture and appliances in the home. And when product recalls are announced, act on them immediately. Visit AnchorIt.gov to see how TV and furniture tip-over incidents occur and the simple steps to prevent them.

Story Source: https://www.cpsc.gov/Recalls/2018/IKEA-Reannounces-Recall-of-MALM-and-Other-Models-of-Chests-and-Dressers-Due-to-Serious-Tip-over-Hazard

Your Baby

Recall: Skip Hop Convertible High Chair

2:00

The U.S. Consumer Product Safety Commission (CPSC,) Health Canada and Skip Hop have recalled the Skip Hop Tuo Convertible High Chair after discovering that the front legs on the highchair can detach from the seat, posing a fall and injury hazard to kids.

The recalled item is the charcoal colored Tuo Convertible High Chair, which converts into a toddler chair.

Consumers with the chair should check for style numbers 304200 and 304200-CN with the date codes HH102016, HH11/2016, HH3/2017 and HH4/2017, which can be found on the back of the chair.

Skip Hop has received 13 reports of the legs of the high chairs detaching, resulting in two reports of bruises to children.  

The Skip Hop Convertible High Chair was sold at Babies ”R” Us, Buy Buy Baby, Target, Kohls, Dillards and other children specialty stores nationwide and online at Amazon.com and Skiphop.com from December 2016 through September 2017 for about $160.

Consumers should immediately stop using the recalled high chairs and contact Skip Hop for a free replacement. 

You can contact Skip Hop toll-free at 888-282-4674 from 9 a.m. to 5 p.m. ET Monday through Friday, or online at www.skiphop.com and click on “Recalls” for more information.

Story source: https://www.cpsc.gov/Recalls/2018/Skip-Hop-Recalls-Convertible-High-Chairs-Due-to-Fall-Hazard

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 Baby

Recall: Oball Baby Rattles Due to Choking Hazard

1:30

About 680,000 Kids ll Inc. Oball baby rattles have been recalled due to choking hazards.

This recall involves Oball Rattles in pink, blue, green and orange with model number 81031 printed on the inner surface of one of the plastic discs and on the packaging. The balls have 28 finger holes and measure four inches in diameter.

Embedded in the rattles are a clear plastic disc with all orange beads and two clear plastic discs with beads of varying colors on the perimeter.

Only rattles with date codes T0486, T1456, T2316, T2856 and T3065 located on a small triangle on the inner surface of the rattle are included in the recall.

The first three numbers represent the day of the year and the last digit represents the year of production.      

The firm has received 42 reports of the plastic disc breaking releasing small beads including two reports of beads found in children’s mouths and three reports of gagging.

Consumers should immediately take these recalled rattles away from young children and contact the firm to receive a full refund.

The rattles were sold at Target, Walgreens, Walmart and other retailers nationwide and online at Amazon.com, Babyhaven.com, Diapers.com, ToysRUs.com, Walgreens.com and other online retailers from January 2016 through February 2017 for between $5 and $7.  

Consumers can contact Kids II toll-free at 877-243-7314 from 8 a.m. to 5 p.m.  ET Monday through Friday or visit www.kidsii.com and click on “Recalls” at the bottom of the page for more information.

Story source: https://www.cpsc.gov/Recalls/2017/Kids-II-Recalls-Oball-Rattles

Daily Dose

Teething Pain & Recalled OTC Products

Do OTC teething products really work? Which ones have been recalled? WHat parents need to know.I am getting a lot of questions from patients related to teething, pain, and the recall of over the counter teething products that contain benzocaine.

The FDA recently issued a warning to parents who use OTC products like Oragel and Anbesol on their infant’s gums for relief of teething pain. These products come as both liquids and gels, and benzocaine is the active pain reducing ingredient. It has now been found that excessive amounts of benzocaine may lead to a very rare, condition called methemoglobinemia. (Hemoglobin is the molecule in the red blood cell that carries oxygen). With methemoglobinemia there is a reduced amount of oxygen that is carried in the bloodstream which may lead to a bluish gray discoloration to the skin, shortness of breath, a rapid heart rate and fatigue and lethargy. Although the FDA did not withdraw these products from the market, they did recommend that they not be used in children under two, and then should be used “sparingly”. Unfortunately, the benzocaine containing products do not yet contain warning labels. I have never recommended using these products in the first place. I always wondered if they really helped a baby who was teething, as I am not sure you can tell when a baby is teething in the first place. If you watch any infant over the age of 4 months, their hands are always in their mouths, and they are constantly drooling!  Does that mean they are getting teeth? Unlikely, as most babies don’t even cut their first tooth until about 6 months, so they have been drooling and putting anything they can in their mouths for months prior. The drooling and “gnawing” on their hands (and sometimes feet too) is rather a developmental milestone and not always a sign of teething. My theory is let the baby chew on a teething ring, a frozen piece of a bagel (cut into quarters, good for gnawing and can throw out when used), or rub their gums with a cold washcloth if you think your child has discomfort. Babies will get teeth for many years to come and once the first several have broken the skin we don’t seem to pay as much attention anyway, right?  I mean, who is going to worry about a child cutting their 2 year old molars, there are way too many other issues to deal with (tantrums, climbing, throwing food) than if their molars are erupting. So, save your money and don’t buy teething products. Now the FDA even agrees! What do you think? I look forward to your feedback.

Your Baby

Recall: 86,000 Osprey Poco Child Backpack Carriers

1:30

Osprey Child Safety Products is recalling 82,000 Poco child carriers after receiving reports that children have fallen from the seats.

Osprey has received four reports of children falling through the carrier leg openings, resulting in one report of a skull fracture and one report of scratches to the head.

This recall involves all models of Poco, Poco Plus and Poco Premium child backpack carriers manufactured between January 2012 and December 2014.  The nylon child carriers were sold in three colors: “Romper Red,” “Koala Grey,” and “Bouncing Blue.” They have a metal frame and a gray padded child’s seat inside. The production date is stamped on a black label sewn into the interior of the large lower zippered compartment on the back of the carrier.

Recalled carriers have a production date code of S12SBPR1, S12SBPR1B, S12SBPR2, S12SBPR3, S12SBPR4, F12SBPR1, F12SBPR2, S13SB IPO, S13SBPR1, S13SBPR2, S13SBPR3, S13SBPR4, F13SBPR1, F13SBPR2, F13SBPR3, S14SBPR1, S14SBPR2, S14SBPR3, S14SBPR4, S14SBPR5. “Osprey” is printed on the fabric above the kickstand. The model name is printed on the back at the bottom.

Consumers should immediately stop using the recalled carriers and contact Osprey for a free Seat Pad Insert for use along with the existing safety straps to secure the child in the carrier. Consumers who previously received and installed the free Seat Pad Insert in their carriers are not required to take further action.

The child carriers were sold at REI and specialty outdoor stores nationwide and online at Amazon.com from January 2012 to December 2015 for between $200 and $300. 

Consumers can contact Osprey, toll-free ,at 866-951-5197 from 8 a.m. to 5 p.m. MT Monday through Friday, email at pocoseatpad@ospreypacks.com or online at www.ospreypacks.com and click on “Poco Safety Notices” on the navigation bar at the top right hand corner of the page for more information.

Story source: https://www.cpsc.gov/Recalls/2017/osprey-recalls-child-backpack-carriers#

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/

 

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!

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