The Recall Desk
SevereFDA (Drugs)·D-400-2013·Announced 2013-05-22

Green Valley Drugs Recalls Polidocanol Injection Due to Sterility Concerns

Green Valley Drugs is recalling Polidocanol Injection vials nationwide due to a lack of assurance of sterility and quality control concerns.

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, which corresponds to a Severe severity score under the rubric for significant injury or health risk potential.

Plain-English summary

FVS Holdings, Inc. dba Green Valley Drugs is recalling 109 vials of Polidocanol Injection, all strengths and presentations, including 5%, 1%, 2%, and 3% concentrations in 30 mL vials. The product is prescription-only and was distributed nationwide.

The recall was initiated due to a lack of assurance of sterility for all sterile products compounded, repackaged, and distributed by the pharmacy. The FDA cited concerns associated with the quality control processes as the reason for the action.

Consumers and healthcare providers should stop using the affected vials and contact their healthcare provider or the recalling firm for further instructions. Specific lot numbers and expiration dates are listed in the official recall documentation.

The recalled product

Product
Polidocanol Injection, all strengths and all presentations including a) Polidocanol 5% 30 mL, b) Polidocanol 1% 30 mL, c) Polidocanol 2% 30 mL, d) Polidocanol 3% 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Manufacturer
FVS Holdings, Inc. dba. Green Valley Drugs
Category
Drug — Injection
Hazard
Affected units
109

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 (6)

  • Lot #: Polidocanol 5% 30 mL: 20130319-I
  • Exp 6/19/2013
  • 20130326-H
  • Exp 6/26/2013
  • b) Polidocanol 1% 30 mL: 20130118-B
  • Exp 4/18/2013

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 →

Related recalls

Same manufacturer · FVS Holdings, Inc. dba. Green Valley Drugs

See all →

Same hazard · sterility

See all →