Recalls: Other Drugs or Medications

January 30, 2018 Walgreens Pain and Itch Relief Cream Recalled by Natureplex Due to Failure to Meet Child Resistant Closure Requirement

The recalled Well at Walgreens Pain and Itch Relief Cream tube and packaging are orange with a purple stripe with "Maximum Strength," "Pain and Itch Relief Cream 4% Lidocaine" and "NET WT 2 OZ (56.7 grams)" printed in white on the front. The Well at Walgreens logo is located on the front upper right corner. The packaging contains the UPC bar code 3 11917 18962 8 on the back. Read more.


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 Assured™. 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.


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.


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.