Recall Z-0174-2019— Life Technologies, Corp.
Class II · Terminated
Class II FDA medical device recall by Life Technologies, Corp., initiated 2018-08-24, terminated 2020-04-29. FDA's recall record names no specific 510(k) clearance for this event. Product: Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061. Reason: Leaky bottles due to a defect in the bottle cap compromising the sterility of the product.
- Recalling firm
- Life Technologies, Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-08-24
- Terminated
- 2020-04-29
- Firm location
- Grand Island, NY, United States
Product description
Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061
Reason for recall
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
Data sourced from openFDA. This site is unofficial and independent of the FDA.