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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: MZB Children’s Watches Due to Rash, Chemical Burns


They are cute, keep time and appeal to children who want to own a watch. But, these watches have a defect that can expose children to serious skin irritations including chemical burns.

Nearly two million MZB Children’s “Light Up” Watches have been recalled because the case-back of the watch can detach and expose the interior to water posing a risk of skin irritation, redness, rashes or chemical burns.

This recall involves 303 styles of “Light Up” watches that are identified by style number. A complete list of the serial numbers is listed on the firm’s website The watches have a flexible plastic wristband sold in multiple colors including pink, pink with white snowflakes, green, blue and navy blue. “MZB” and the style number are printed on the case-back of the watches.

The firm has received 11 reports of skin irritations or chemical burns. Six of these consumers have required medical treatment.

The watches were sold at Kmart, Kohl’s, Walmart and other retailers nationwide from October 2012 through June 2015 for between $5 and $20.

Consumers should immediately take the recalled watches away from children and contact MZB for a refund.

MZB can be reached by calling their toll free number at (888) 770-7085 from 8 a.m. to 7 p.m. ET Monday through Friday or online at and click on Product Safety Notice tab at the top of the homepage for more information.



Recall: Cracker Barrel’s Animated Toy Monkey Due to Burns


Giggles International is recalling about 13,000 of their Animated Sing Along Monkey toy due to the possibility that the battery compartment can reach temperatures up to 230 degrees Fahrenheit, posing a burn hazard for children.

This recall involves Giggles International Animated Sing-Along Monkey toys. The monkey is made of brown and beige plush material and is about 9 inches tall. The toy is designed to hold a songbook titled "5 Little Monkeys" and to sing the song when activated. A red music note is on the bottom of the monkey's right foot and the face of a child with its hands covering its eyes are on the bottom of the money's left foot. Recalled sing-along monkeys were manufactured between 6/7/2014 and 7/5/2014 and have batch code GP1410028.  

The manufacture date in the M/D/YYYY format and batch code are printed on the bottom of a white fabric label attached near the base of the monkey's tail. The monkey toys came in a tan colored box with words "Animated Sing-Along Monkey," "Sing along with me!" and "I play peek-a-boo with you!" on the front. The age advisory "For ages 3+" and the warning that batteries are included are also on the front of the box.

Giggles International has received two reports of toys overheating and melting their battery compartments.

The toy is sold exclusively at Cracker Barrel Old Country Stores nationwide from September 2014 to October 2014 for about $25.

Consumers should immediately take the animated monkey away from children, remove the batteries and return the toy to any Cracker Barrel Old Country Store or contact Giggles International for a full refund.

You can contact Giggles International at (800) 738-6018 from 9 a.m. to 6 p.m. ET Monday through Friday or online at and click on Recall at the top of the page for more information.

Toy monkey recall

Your Baby

Recall: DaVinci Baby Cribs


Bexco has expanded a recall of their baby cribs. Bexco recalled an additional 11,600 cribs in July 2015.

The firm has received five additional reports of the mattress support brackets breaking and detaching. No injuries have been reported.

A metal bracket that connects the mattress support to the crib can break, creating an uneven sleeping surface or a gap. If this occurs, a baby can become entrapped in the crib, fall or suffer lacerations from the broken metal bracket.

This recall includes DaVinci brand full-size cribs including the Reagan crib (model #M2801), the Emily crib, (model #M4791), the Jamie crib (model #M7301), and the Jenny Lind crib (model #M7391) manufactured from May 2012 through December 2012.

The model number, serial number and manufacture date are printed on a label affixed to the bottom right hand side panel of the crib. Cribs included in the recall have serial numbers that begin with “N00,” followed by one of the following numbers.  The previous recall included the same model numbers, but had different serial numbers.

The cribs were sold at Target and juvenile products stores nationwide and online at from May 2012 to December 2013 for between $150.00 and $250.00.

Consumers should immediately stop using the recalled cribs and contact Bexco for a free replacement mattress-support that includes replacement brackets.  In the meantime, parents are urged to find an alternate, safe sleeping environment for the child, such as a bassinet, play yard or toddler bed depending on the child’s age.

Consumers can contact DaVinci toll-free at 888-673-6652 from 8:30 a.m. to 5:15 p.m. PT Monday through Friday. Consumers can also visit or and click on “Safety Recall” for more information.


Your Baby

IKEA Recalls 169,000 Crib Mattresses


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


·      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 and click on the recall link at the top of the page for more information.



Kidde Recalls 4.6 Million Fire Extinguishers


A lot of families have fire extinguishers in their homes in case of a small fire. Kidde makes one of the more popular brands and is recalling 4.6 million of their plastic valve disposable fire extinguishers.

A faulty valve component can cause the disposable fire extinguishers not to fully discharge when the lever is repeatedly pressed and released during a fire emergency, posing a risk of injury.

This recall involves 31 models of Kidde disposable fire extinguishers with Zytel® black plastic valves. The recalled extinguishers are red, white or silver and are either ABC or BC rated. The ratings can be found to the right of the nameplate. 

Manufacture dates included in the recall are July 23, 2013 through October 15, 2014. A 10-digit date code is stamped on the side of the cylinder, near the bottom. Digits five through nine represent the day and year of manufacture in DDDYY format.

Date codes for recalled units manufactured in 2013 are XXXX 20413 X through XXXX 36513 X and 2014 are XXXX 00114 X through XXXX 28814 X.

A complete list of the nameplate affixed to the front of the fire extinguishers is located on their website at

Kidde has received 11 reports of the recalled fire extinguishers failing to discharge as expected. No injuries have been reported.

The fire extinguishers were sold at Home Depot, Menards, Walmart and other department, home and hardware stores nationwide, and online from August 2013 through November 2014 for between $18 and $65, and about $200 for model XL 5MR.

Consumers should immediately contact Kidde for a replacement fire extinguisher at Kidde toll-free (855) 283-7991 from 8 a.m. to 5 p.m. ET Monday through Friday, or online at and click on Safety Notice for more information.

Your Child

PetSmart Expands Fish Bowl Recall Due to Lacerations


PetSmart is expanding its recall of fishbowls after several injury reports.

The glass fishbowls can crack, shatter or break during normal handling, posing a laceration hazard to consumers.

This recall involves the 1.75-gallon glass fishbowl that is shaped like a brandy snifter. These fishbowls were sold under the Grreat Choice or Top Fin brand names with SKU number 5140161 and UPC code 737257187092. The SKU and UPC codes are printed on a white sticker on the bottom of the fishbowl.

PetSmart has received 20 new reports of the glass fishbowl breaking during normal use, including 14 additional reports of cuts to fingers and hands. Seven cuts required stitches and three others required surgery for lacerated tendons.  

About 81,300 of these fishbowls were sold exclusively at PetSmart stores and online from March 2010 through September 2013 for about $20.

This recall comes on the heal of a previous recall involving the Top Fin Betta Bowl Kit.

Bowls can break, crack or shatter with normal use.

The Top Fin Betta Bowl Kits with LED Lights include a 0.6-gallon glass betta bowl and a base with an LED light. The plastic bases come in black, blue, pink, purple and silver. The following UPC numbers are located on the packages of recalled items.


Black- UPC: 73725752848

Blue- UPC: 73725747577

Blue- UPC: 73725747577

Pink-UPC:  73725747595 

Purple            - UPC: 73725752855

Silver- UPC: 73725747598

The firm has received seven reports of incidents, including five reports of cuts to fingers and hands.

About 148,000 bowls were sold in the United States.

The fishbowls were sold exclusively at PetSmart stores nationwide and online at from September 2013 through October 2015 for about $25.

Consumers should immediately stop using the fish bowls and return the fish bowl to any PetSmart store for a full refund. Use caution when handling the fish bowl for return due to the hazard. 


Your Baby

Recall: 2-in-1 Dream On Me Bassinet to Cradle


Dream on Me is recalling about 13,000 of their 2-in-1 Bassinet to Cradle products due to fall and suffocation hazards.

The wire supports on the sides of the bassinet can disconnect causing the fabric sides to lower; posing a risk that infants can fall out or become entrapped and suffocate.

This recall involves the 2-in-1 Bassinet to Cradle, sold in pink, blue, green, and white. The bassinet has metal frame supports and fabric sides with a removable half-canopy on the top.  The frame can also be adjusted with two rocking legs on each end of the bassinet.

It is designed with fabric handles and the option to remove the bassinet from the frame to use the bassinet portion as a “by the bed” sleeper product.

The recalled model numbers are:

·      439-A

·      439-B

·      439-G

·      439-P

·      439-W

The model numbers can be found on a tag that is located under the mattress pad of the bassinet. This tag is a removable tag you see in the store but is removed prior to use.

Dream on Me has received one incident of the wire frame support bracket failing and the fabric portion of the bassinet collapsing while an infant was asleep in the cradle.  No injuries have been reported.  

Consumers should immediately stop using the product and contact Dream On Me to obtain a free repair. In the meantime, parents are urged to find an alternate, safe sleeping environment for the child, such as a crib that meets current safety standards or play yard depending on the child’s age.

The recalled products were sold online at,,, and from May 2012 to October 2014 for about $60.

Consumer can contact Dream on Me toll-free at (877) 201-4317, from 9 a.m. to 4:30 p.m. ET Monday through Friday, or online at and click on the “Recalls” icon on the home page for more information.


Your Child

Recall: Children’s Cough Syrup


Parents are being urged to check their medicine cabinets as two batches of generic children's cough syrup are removed from pharmacy shelves across the country. They have been recalled due to overdose risk.

The voluntary recall was initiated after it was discovered the dosage cups included in the box had incorrect markings, leading to fears that children may be given too much medication, according to a statement from the manufacturer.

The products in question are:

·      Children's guaifenesin grape liquid (100mg/5 mL)

·      Children's guaifenesin DM cherry liquid (100mg guaifenesin and 5mg dextromethorphan HBr/ 5 ml) sold in 4 oz. bottles

Each includes a small plastic cup.                  

The over-the-counter cough syrups are sold generically nationwide, under different brand names:


·      H.E.B

·      CVS


·      Sunmark

•       Rite-Aid

•       Topcare

•       Kroger

•       GoodSense

•       Dollar General

•       Care One

•       CVS

The U.S. Food and Drug Administration said it is aware of the voluntary recall and urged consumers who bought the batches listed above "to discard the dosing device and product."

While there have been no reported overdoses related to the medication, the Perrigo Company said side effects of an overdose can include "hyperexcitability, rapid eye movements, changes in muscle reflexes, ataxia, dystonia, hallucinations, stupor and coma," adding that other effects have included "nausea, vomiting, tachycardia, irregular heartbeat, seizures, respiratory depression and death."

Source: Amy La Porte,


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