The Recall Desk
SevereFDA (Drugs)·D-1034-2013·Announced 2013-09-18

Wellness Pharmacy Recalls RL Glutathione Due to Sterility Concerns

Wellness Pharmacy is recalling RL Glutathione 100 mg/mL vials due to laboratory results indicating microbial contamination and concerns about the reliability of testing.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II and involves microbial contamination of a sterile injectable product, which poses a significant risk of harm and fits the 'Severe' criteria for significant injury reports or high-risk contamination.

Plain-English summary

Wellness Pharmacy, Inc. is recalling specific lots of RL Glutathione 100 mg/mL, SDV PF, in 1 mL, 2 mL, 3 mL, and 4 mL vial sizes. The recall involves 34 vials from Lot # 130710@27, which has a use-by date of 1/6/2014. The product was distributed nationwide and in Puerto Rico.

The recall was initiated due to laboratory results indicating microbial contamination. Additionally, the FDA expressed concern that test results obtained from the recalling firm's contract testing laboratory may not be reliable, leading to a lack of assurance regarding the sterility of the product.

Consumers who have purchased this product should stop using it and contact Wellness Pharmacy at 1-800-227-2627 for further instructions.

The recalled product

Product
RL Glutathione 100 mg/mL, SDV PF,a) 1 mL, b) 2 mL, c) 3 mL, and d) 4 mL, WELLNESS PHARMACY, 1-800-227-2627
Affected units
34

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot# 130710@27
  • Use By: 1/6/2014

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 6 recalled by Wellness Pharmacy, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →