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aap Implantate AG · Model IS 3305-24 · UDI-DI 04042409452864
HWW
Prescription
0
510(k) clearances
15
Adverse events
17
Recalls
112
Facilities
Description
Countersink Ø6.2, cannulated, I-Ø2.6, L 120, Hudson coupling
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| 2019-04-08 | Zimmer GmbH | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
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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.
