Recalls: Drugs and Cosmetics

November 30, 2017 Natural Solutions for Life Recalls Synodrin Pain Relieving Cream Due to Failure to Meet Child Resistant Closure Requirement

The recalled Synodrin Lidocaine Maximum Strength Pain Relieving Cream is in a white jar with a blue label with "Synodrin Lidocaine Maximum Strength 4% Pain Relieving Cream" printed on the front. The jars measure about three inches in diameter, are three inches tall and weigh about 4 ounces. They were sold in a blue box with yellow letters "Lidocaine" and white letters "Maximum Strength 4% Pain Relieving Cream." The brand name Synodrin is printed on the jar and the box. The box and jar have UPC code 8 64751 00032 6 printed on the right side. Read more.


December 10, 2015 Dollar Tree Recalls Burn Relief Gel Due to Failure to Meet Child Resistant Closure Requirement

The recalled burn relief gel is packaged in a blue box with white letters "Burn Relief" and red letters "Burn Relief Gel". The brand name is Assuredâ„¢. Inside the box is a blue and white tube labeled "Burn Relief Gel" and measuring approximately 5 inches long by 1 inch wide and weighs about 0.7 ounces (20 grams). The packaging contains the UPC bar code: 6 39277 09311 0. Read more.


August 18, 2015 Merck Recalls Temodar and Temozolomide Bottles with Cracked Caps Due to Failure to Meet Child-Resistant Closure Requirement

This recall to replace involves bottle caps for Temodar and Temozolomide (generic) capsules, an oral chemotherapy drug. The capsules were distributed in 5- and 14-count brown glass bottles that have white plastic child-resistant caps. A white label affixed to the bottle has the word "Temozolomide" printed in black lettering. Read more.


July 14, 2014 GSK Recalls Panadol Advance Bottles Due to Failure to Meet Child-Resistant Closure Requirement; Sold Exclusively in Puerto Rico

This recall involves bottles of 100ct Panadol Advance pain relievers. The medicine was sold in white containers with a blue label, inside a blue box. "Panadol" and "Advance" are printed on the label. Lot numbers and dates codes are located on the left side panel of the box and on the left side of the label on the bottle, near the bar code. Lot numbers and date codes included in the recall are: Lot number: 14241, expiration date: 02/2015 Lot number: 14002, expiration date: 10/2014 Lot number: 13881, expiration date: 09/2014 Lot number: 13801, expiration date: 09/2014 Read more.


May 13, 2014 Avon Recalls Ergonomic Eyelash Curler Due to Eye Injury Hazard

This recall involves an Avon Ergonomic Eyelash Curler which is silver with black ergonomic finger grips. The word Avon is engraved in the silver upper lash curling bar. The recalled curler has the Avon model number F3093441 which can be found on the product's box. Read more.


January 31, 2013 FoodState Recalls Bottles of MegaFood One Daily Supplements Due to Lack of Child-Resistant Packaging

The recalled supplement bottles are brown glass bottles that contain MegaFood One Daily Tablets. The bottles have a yellow label on the front with the words "MegaFood," "Fresh From Farm To Tablet," "One Daily," "Nourish," "Balance" and "Replenish" printed above a picture of vegetables. Recalled bottles have the following amounts, product codes and lot numbers:

Amount

Product Code

Lot Numbers

60 tablets

51494 10151

10613, 10724 through 10728, 11246 and 12191

90 tablets

51494 10152

180 tablets

51494 10153

The amount is on the bottom right of the front label. The product code and lot numbers are on the left side of the front label.

Read more.


June 23, 2011 Rugby Children's Pain & Fever Concentrated Drops Recalled Due To Failure to Meet Child-Resistant Closure Requirement

The recall involves Rugby Children's Pain & Fever Concentrated Drops (Acetaminophen Drops) in a 1/2 fl. oz. (15 ml) bottle size. The UPC code 305361936723 can be found with the bar code at the bottom of the box. The affected lot numbers are: Read more.


June 25, 2010 Scope® Original Mint Mouthwash Recalled by Procter & Gamble Due to Failure to Meet Child-Resistant Closure Requirement

This recall involves some bottles of Scope® Original Mint Mouthwash in 1 liter sizes. The recalled bottles have the number 4 on the bottom of the bottle. The bottles with the 4 on the bottom may not be child-resistant. Consumers can also attempt to twist the cap open. If the cap can be twisted off without squeezing the tabs on the cap, the package is not child-resistant. Read more.


December 18, 2009 Vicks Dayquil Cold & Flu Liquicaps Recalled by Procter & Gamble Due To Failure to Meet Child-Resistant Closure Requirement

The recall involves Vicks Dayquil Cold & Flu 24-Count Bonus Pack Liquicaps. The medicine comes in orange packaging with the green Vicks symbol and has the following UPC#: 3 23900 01087 1. No other Vick’s product is included in this recall. Read more.


July 10, 2008 Lip Gloss and Jewelry Sets Sold Exclusively at Wal-Mart Recalled by F.A.F. Inc. Due to Risk of Lead Exposure

The recalled three-piece sets contain a rectangle-shaped lip gloss container, a heart-shaped locket necklace, and a charm bracelet. The following models are included in the recall: Read more.