NA
Fehling Instruments GmbH & Co. KG · Model MOA-8 · UDI-DI 04058749000085
DWZ
Prescription
1
510(k) clearances
89
Adverse events (1 deaths)
1
Recalls
24
Facilities
Description
Biopsy forceps, single use sterile, 1,8 x 1.200 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-12 | Heartport, Inc. | Guidewire is protruding through the film portion of the packages which compromises the sterility of the device. |
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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.