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KCQ5 COMPLEMENT – LONG DRILLS
BIOTECHNOLOGY INSTITUTE SL · Model KCQ5-2 · UDI-DI 08435389826569
OFY
Prescription
0
510(k) clearances
0
Adverse events
1
Recalls
22
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-05-18 | Zimmer Inc. | The instructions for use contain pre-vacuum sterilization instructions that may lead to compromised sterility at the lid-kit interface location. |
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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.
