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PRIMA
LIMACORPORATE SPA · Model 9013.67.020 · UDI-DI 08033390214797
10
510(k) clearances
10,195
Adverse events (34 deaths)
19
Recalls
216
Facilities
Description
PRIMA - Humeral Starting Awl
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-09 | Exactech, Inc. | Potential for incorrect Instructions For Use (IFU) included with an Equinoxe Humeral Stem, Primary, Press Fit, 11mm package. |
| 2018-11-16 | Ascension Orthopedics, Inc | The product was packaged with the Instructions for Use for a different product (Ascension First Choice DRUJ System Partial Ulnar Head Implant). |
| 2018-06-04 | Fx Solutions | Breach in the external blister of certain lots of Humelock Offset Head 50 X 20 and Centered Head 50 X 19. |
| 2018-06-04 | Fx Solutions | Breach in the external blister of certain lots of Humelock Offset Head 50 X 20 and Centered Head 50 X 19. |
| 2017-12-08 | Zimmer Biomet, Inc. | Zimmer Biomet is conducting a medical device recall for two lots of Comprehensive Humeral stems. The lots were commingled during the manufacturing process and were etched with inco |
| 2017-12-08 | Zimmer Biomet, Inc. | Zimmer Biomet is conducting a medical device recall for two lots of Comprehensive Humeral stems. The lots were commingled during the manufacturing process and were etched with inco |
| 2017-08-31 | DePuy Orthopaedics, Inc. | The affected lots are being recalled because the epiphysis may not assemble to the stem, which may cause a surgical delay. |
| 2015-08-14 | Limacorporate S.p.A | The dimensions of the mating features of the recalled products are out of specification causing the device to be difficult to assemble. |
| 2014-11-24 | Arthrosurface, Inc. | Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications. |
| 2014-11-24 | Arthrosurface, Inc. | Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications. |
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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.
