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MEM Earles
LIFE TECHNOLOGIES CORPORATION · Model 11095072 · UDI-DI 10190302001663
KIT
Prescription
10
510(k) clearances
5
Adverse events
4
Recalls
25
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-08-24 | Life Technologies, Corp. | Leaky bottles due to a defect in the bottle cap compromising the sterility of the product |
| 2018-08-24 | Life Technologies, Corp. | Leaky bottles due to a defect in the bottle cap compromising the sterility of the product |
| 2018-08-24 | Life Technologies, Corp. | Leaky bottles due to a defect in the bottle cap compromising the sterility of the product |
| 2018-08-24 | Life Technologies, Corp. | Leaky bottles due to a defect in the bottle cap compromising the sterility of the product |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.