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Procure™

ST. JUDE MEDICAL, INC. · Model 408297 · UDI-DI 05415067009555

DWZ Prescription
1
510(k) clearances
89
Adverse events (1 deaths)
1
Recalls
24
Facilities

Description

Endomyocardial Biopsy Forceps

Recalls

DateFirmReason
2005-04-12Heartport, Inc.Guidewire is protruding through the film portion of the packages which compromises the sterility of the device.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.