Agency classClass IIOur severity:Severe FDA (Drugs)·D-1503-2015·Announced 2015-09-23

Glutathione Injection Recalled for Lack of Sterility Assurance

The Compounding Pharmacy of America is recalling Glutathione 200 mg/ml Injection due to FDA inspection findings of GMP violations that may impact sterility.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The source text explicitly states the agency classification is Class II. Per the rubric, FDA Class II recalls are mapped to a severity score of 4 (Severe), particularly given the risk to sterility in an injectable product.

Plain-English summary

The Compounding Pharmacy of America is recalling Glutathione 200 mg/ml Injection, Multi-Dose Vial, Sterile, Refrigerate. The recall involves 559 ml total volume of product distributed nationwide between November 2014 and May 2015. Specific lot codes and expiration dates are listed in the recall documentation.

The recall was initiated because an FDA inspection identified Good Manufacturing Practice (GMP) violations that potentially impact product quality and sterility. The agency has classified this as a Class II recall, indicating a reasonable probability that use of the product could cause temporary or medically reversible health consequences.

Consumers and healthcare providers should stop using the recalled product and contact the recalling firm or their healthcare provider for instructions on return or disposal. No specific illnesses or injuries have been reported in the source text.

The recalled product

Product: Glutathione 200 mg/ml Injection, Multi-Dose Vial, Sterile, Refrigerate, The Compounding Pharmacy of America, Knoxville, TN
Manufacturer: The Compounding Pharmacy of America
Category: Drug — Injectable
Hazard: sterility
gmp-violation

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 (14)

All lots distributed between November 2014 and May 2015
03162015@78
6/14/2015
03262015@42
6/24/2015
04202015@82
7/19/2015
04222015@79
7/21/2015
05042015@49
8/2/2015
04222015@57
04272015@19
7/26/2015

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 382 recalled by The Compounding Pharmacy of America 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 382 products in this recall →

Same manufacturer · The Compounding Pharmacy of America

See all →

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Same hazard · sterility