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EBERLE
Eberle GmbH & Co. KG · Model 900312 · UDI-DI 04050052027971
4
510(k) clearances
102
Adverse events
1
Recalls
1
Facilities
Description
Immersion basket
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-01-18 | Stryker Spine | Stryker Spine received reports of packaging failures during shipping for the Jam Shidi instruments, which may compromise 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.