Home › DIAGNOSTIC HYBRIDS, INC. › ELVIS
ELVIS
DIAGNOSTIC HYBRIDS, INC. · Model 10-220500 · UDI-DI 30014613331209
KIT
Prescription
10
510(k) clearances
5
Adverse events
4
Recalls
25
Facilities
Description
ELVIS REPLACEMENT MEDIUM
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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.