FDA Device recall Z-0174-2019
Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061
- FDA Device
- Class II
- terminated
- Published 2018-10-24
On 2018-10-24 the FDA classified a Class II recall of Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061 by Life Technologies, citing leaky bottles due to a defect in the bottle cap compromising the sterility of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0174-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-08-24 |
| Published | 2018-10-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Life Technologies |
| Distribution | US |
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
Identifiers
| code_info | Lot Number: 1967697 (UDI 10190302001823) Exp. Date: 30-Jun-2020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0174-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.