The Recall Desk
SevereFDA (Drugs)·D-350-2013·Announced 2013-05-22

Green Valley Drugs Recalls Biotin Injection Due to Sterility Concerns

Green Valley Drugs is recalling Biotin Injection products because the pharmacy could not ensure the sterility of the compounded items.

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 the hazard involves a lack of sterility assurance in injectable products, which poses a significant risk of serious injury or infection.

Plain-English summary

FVS Holdings, Inc. dba. Green Valley Drugs is recalling Biotin Injection, all strengths and all presentations, including Biotin-15-30 mL. The recalled products are prescription-only and were distributed nationwide. The specific lot number is 130117500AE with an expiration date of 4/17/2013.

The recall was initiated due to a lack of assurance of sterility. The source text indicates that all sterile products compounded, repackaged, and distributed by this compounding pharmacy are affected due to concerns associated with the quality control processes.

Consumers and healthcare providers should stop using the recalled Biotin Injection products and contact their healthcare provider or the recalling firm for further instructions.

The recalled product

Product
Biotin Injection, all strengths and all presentations including Biotin-15-30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Affected units
7

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 #: 130117500AE
  • Exp 4/17/2013

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 78 recalled by FVS Holdings, Inc. dba. Green Valley Drugs 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 78 products in this recall →