The Recall Desk
ModerateFDA (Devices)·Z-2423-2017·Announced 2017-06-21

Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards

Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, leading to antibiotic degradation.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically indicates a temporary or medically reversible adverse health consequence. The hazard is a loss of potency due to moisture exposure, which is a functional defect rather than a direct physical injury or acute toxicity risk, fitting the Moderate severity criteria for low-risk contamination or functional issues without reported illness.

Plain-English summary

Biomerieux Inc is recalling 2,187 cartons of VITEK 2 Gram Negative Susceptibility cards (AST-GN84), REF 413410. The recall involves 20 cards per carton.

The recall was initiated because the integrity of the product container may be compromised. This exposure to moisture could lead to antibiotic degradation and a loss of potency.

The product was distributed nationwide in the U.S., including military and government sites, as well as to numerous international locations. The source text does not specify instructions for consumers or healthcare providers regarding the disposition of the recalled product.

The recalled product

Product
VITEK¿ 2 Gram Negative Susceptibility card (AST-GN84), REF 413410, 20 cards per carton.
Manufacturer
Biomerieux Inc
Affected units
2,187

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)

  • 6740247103 31/Jul/18 6740272203 25/Aug/18

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 187 recalled by Biomerieux Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 187 products in this recall →