Class II — Life Technologies, Corp.
| Recalling firm | Life Technologies Corporation |
|---|---|
| Registered facility | View this company's 9 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Leaky bottles due to a defect in the bottle cap compromising the sterility of the product |
| Product | Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061 |
| Quantity | 1912 units |
| Distribution | Nationwide: Foreign: Argentina Australia Canada China Great Britain Hong Kong India Japan Mexico Netherlands New Zealand Singapore South Korea Taiwan |
| Initiated | 2018-08-24 |
| Classified | 2018-10-17 |
| Terminated | 2020-04-29 |
| Recall number | Z-0174-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Life Technologies, Corp. (Z-0174-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81052/
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