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SparrowHawk
ATC TECHNOLOGIES, INC. · Model 5030 · UDI-DI 00817428020189
DWZ
Prescription
1
510(k) clearances
89
Adverse events (1 deaths)
1
Recalls
24
Facilities
Description
5030 SparrowHawk Endomyocardial Biopsy Forceps, 2.2mm X 50cm, Max-Curve, Disposable
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.