The Recall Desk
SevereFDA (Drugs)·D-399-2013·Announced 2013-05-22

Green Valley Drugs Recalls Phosphatidylcholine Injection Due to Sterility Concerns

Green Valley Drugs is recalling Phosphatidylcholine and Sodium Deoxycholate Injection due to a lack of assurance of sterility in compounded products.

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 rating under the rubric, particularly given the risk of infection from non-sterile medical products.

Plain-English summary

FVS Holdings, Inc. dba. Green Valley Drugs is recalling Phosphatidylcholine and Sodium Deoxycholate Injection, all strengths and all presentations, including Phospha_Deoxy-35-30-50 mL. The recall involves 40 vials distributed nationwide. The specific lots affected are 201303071500JN (Exp 6/7/2013) and 1301231000AE (Exp 4/23/2013).

The recall was initiated due to a lack of assurance of sterility in 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 products and contact their healthcare provider or the recalling firm for further instructions.

The recalled product

Product
Phosphatidylcholine and Sodium Deoxycholate Injection, all strengths and all presentations including Phospha_Deoxy-35-30-50 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Manufacturer
FVS Holdings, Inc. dba. Green Valley Drugs
Category
Drug — Injectable
Hazard
Affected units
40

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 (4)

  • Lot #: 201303071500JN
  • Exp 6/7/2013
  • 1301231000AE
  • Exp 4/23/2013

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 →

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

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Same hazard · sterility

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