PERSONA The Personalized Knee System Constrained Tibial Articular… — Class II medical device recall Z-2575-2014
Terminated recall by Zimmer, Inc., reported 2014-09-10, distributed nationwide. Reports of breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). The Persona primary knee
| Recall number | Z-2575-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-08-07 |
| Classified | 2014-09-04 |
| Reported by FDA | 2014-09-10 |
| Terminated | 2015-01-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, CH, DE, ES, FR, GB, IL, IN, IT, JP, KR, LU, NL, SA, SG, ZA |
| Quantity | 77,737 units |
| Reason classes | device malfunction |
| Lot numbers | 62345370, 62347233, 62347240, 62351310, 62352330, 62357328, 62357329, 62357865, 62357866, 62358632, 62358633, 62363685, 62364505, 62372411, 62373739, 62373740, 62374803, 62399612, 62399870, 62402721, 62405896, 62406970, 62407568, 62407772, 62410788, 62410789, 62410790, 62412999, 62416376, 62423921, 62423922, 62424796, 62424804, 62428432, 62430403, 62432150, 62432152, 62432154, 62432157, 62432790 and 63 more |
| Model numbers | 42517600303, 42517600313, 42517600505, 42517600515, 42517600707, 42517600717, 42517600909, 42517600919, 42527600303, 42527600313, 42527600505, 42527600515, 42527600707, 42527600717, 42527600909, 42527600919 |
Product
PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD +0MM; L CD +6MM; L EF +0MM;L EF +6MM; L GH +0MM; L GH +6MM; L J +0MM; L J +6MM; R CD +0MM; R CD +6MM; R EF +0MM; R EF +6MM; R GH +0MM; R GH +6MM; R J +0MM; R J +6MM; and
Reason for recall
Reports of breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). The Persona primary knee surgical technique has been updated. This field action correction is to ensure that all distributors and users of this instrument are aware of the enhanced surgical techniques.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2575-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.