The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-0337-2016·Announced 2015-11-25

Downing Labs Recalls L-Glutamine Injectable Due to Sterility Concerns

Downing Labs, LLC is recalling L-Glutamine Injectable vials because the company cannot assure the product's sterility. The recall covers all lots distributed in the US and internationally.

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 recall is classified as FDA Class II. According to the rubric, an FDA Class II recall involving a significant hazard such as lack of sterility assurance in an injectable drug warrants a score of 4 (Severe), as it poses a risk of serious injury or death if contaminated.

Plain-English summary

Downing Labs, LLC is recalling 14 vials of L-Glutamine Injectable, 30mg/mL, 30mL vial, Rx only. The recall is being conducted because the company lacks assurance of the product's sterility. The affected product is distributed nationwide in the US and in several international locations, including Australia, Brazil, and Japan.

The recall covers all lots of the product. The source text does not specify a particular date range or specific lot numbers beyond the indication that all lots are affected. No illnesses or injuries are reported in the source text.

Consumers and healthcare providers should stop using the recalled product and contact Downing Labs, LLC at 1-800-914-7435 for further instructions or to arrange a return.

The recalled product

Product
L-Glutamine Injectable, 30mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Manufacturer
Downing Labs, LLC
Category
Drug — Injectable
Hazard
Affected units
14

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 (1)

  • All lots

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 48 recalled by Downing Labs, LLC 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 48 products in this recall →

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