RECALL ALERT: Cradle Gliders Recalled Due to Infant Fall Hazard

Dream On Me Recalls Cradle Gliders Due to Infant Fall Hazard
Consumers should stop using this product unless otherwise instructed.
Recall date: November 13, 2013

Hazard:
The mattress support board can fall out or slide out of the bottom of the cradle glider posing a risk that babies can fall out and suffer injuries.




Incidents/Injuries
Dream On Me and CPSC have received reports of two incidents while infants were asleep inside the cradle. A one-month old infant fell to the floor when the mattress support board partially fell out, but the child was uninjured. A second report involved a four-month old infant who did not fall out of the cradle after the mattress support board became partially disengaged.

If you have been injured due to a defective product call the experienced product liability lawyers at Buttafuoco & Associates 1-800-669-4878

Baby Thrown From 2nd Floor Apartment Windown Survives

A 58-year-old woman, Arlene Pickett, was killed in an apartment fire in Ambridge over the weekend.  She was attempting to get out of the burning building and was found in a stairwell.

Neighbors said they saw smoke pouring out of the windows and could hear people screaming from inside.
 “It was amazing, little kids crying for their mother. It was terrible, terrible. The flames were coming straight out like a furnace,” witness Mike Vougias said.

People living nearby said they piled up mattresses so those trapped could jump to safety. A baby was also thrown out the window and was safely caught by a man standing by.

“We grabbed the mattresses and piled them up below the window and they jumped out one-by-one and tossed the baby down,” neighbor Siera Mixter said.

 “The mother finally jumped out first. The dad threw the baby out. There was a gentleman that caught the baby,” witness A.J. Mixter said.

“I caught the baby. I just put my arms out and he fell into my arms,” Bob Dunn said.

RECALL ALERT: Perrigo Recalls Acetaminophen Infant Liquid Due to Syringe Error

PERRIGO INITIATES NATIONWIDE VOLUNTARY PRODUCT RECALL OF ACETAMINOPHEN INFANT SUSPENSION LIQUID, 160 mg/5 mL, DUE TO A POTENTIAL DEFECT WITH THE CO-PACKAGED ORAL SYRINGE

The Perrigo Company (NYSE: PRGO; TASE) announced today that it has initiated a voluntary, nationwide product recall to the retail level of 18 batches of its acetaminophen infant suspension liquid, 160 mg/5 mL, sold in 2 oz. and 4 oz. bottles with syringes in a box under the store brand products listed below. The recall is being initiated because of the remote potential that a small number of packages might contain an oral dosing syringe without dose markings. The correct syringe should have a white or yellow plunger with specific dose markings for 1.25 ml, 2.5 mL, 3.75 mL, and 5 ml. If the product's syringe has these dose markings, consumers can continue to use the product while following labeled use instructions.

Using an oral syringe without dose markings can result in inaccurate dosing, especially in infants who could mistakenly get too high a dose.

     Commenting on this market action, Perrigo's Chairman, President and CEO Joseph C. Papa stated, "There are no issues or concerns with respect to the safety or efficacy of the product, only the potential that the oral dosing device in a relatively small number of packages could be unmarked. Out of an abundance of caution, we are taking this measure to maintain the highest possible product quality standards for our retail customers and consumers. While we cannot be certain that any of these unmarked dosing devices were released into our customers' supply chains, taking this action is the right thing to do." Perrigo has not received any reports or complaints related to this defect nor have they found any product with missing dose markings on re-examination of product on hand.

     This OTC product is indicated for the relief of fever and minor aches and pains and can be used in infants, children and adults. These recalled products are sold by distributors Nationwide and distributed through retail stores.

     Perrigo is notifying its distributors and customers by verbal and e-mail communication today, followed by formal Fed Ex-delivered communication. It also is arranging for return of all recalled products. Distributors/retailers that have the acetaminophen infant suspension liquid that is being recalled should stop distribution and return product.

     If the oral dosing device contained in the package has dose markings, no action is required, and the consumer can continue to use the product consistent with the label instructions. If the package contains an oral dosing device that does not have dose markings, the consumer should not use the product and should call Perrigo's Consumer Affairs Department, toll free, 1-800-719-9260. Consumers should contact their physician or health care provider if they have any questions, or if they or their children experience any problem that could possibly be related to this drug product.


If you or someone you know has been injured due to a defect product call the experienced product liability attorneys at Buttafuoco & Associates 1-800-669-4878