Persona — Class II medical device recall Z-2297-2014
Terminated recall by Zimmer, Inc., reported 2014-08-27, distributed nationwide. Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals
| Recall number | Z-2297-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2013-06-10 |
| Classified | 2014-08-21 |
| Reported by FDA | 2014-08-27 |
| Terminated | 2014-09-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, IN, JP, KR, SG |
| Quantity | 70,986 distribution |
| Reason classes | device malfunction |
| Lot numbers | 62019862, 62022340, 62022342, 62024973, 62024974, 62024977, 62029578, 62030854, 62030862, 62032099, 62036671, 62043562, 62043563, 62046410, 62050136, 62055685, 62055687, 62062232, 62075271, 62075277, 62087042, 62089764, 62091183, 62091198, 62091814, 62104367, 62104420, 62125572, 62125573, 62125597, 62125598, 62144791, 62144797, 62149177, 62149716, 62154284, 62165540, 62165542, 62165544, 62166222 and 333 more |
| Model numbers | 42517000303, 42517000313, 42517000505, 42517000515, 42517000707, 42517000717, 42517000909, 42517000919, 42527000303, 42527000313, 42527000505, 42527000515, 42527000707, 42527000717, 42527000909, 42527000919 |
Product
Persona (TM) The Personalized Knee System Tibial Articular Surface Provisional Bottom Nonsterile TASP L CD BOTTOM, +0MM TASP L CD BOTTOM, +6MM TASP L EF BOTTOM, +0MM TASP L EF BOTTOM, +6MM TASP L GH BOTTOM, +0MM TASP L GH BOTTOM, +6MM TASP L J BOTTOM, +0MM TASP L J BOTTOM, +6MM TASP R CD BOTTOM, +0MM TASP R CD BOTTOM, +6MM TASP R EF BOTTOM, +0MM TASP R EF BOTTOM, +6MM TASP R GH BOTTOM, +0MM TASP R GH BOTTOM, +6MM TASP R J BOTTOM, +0MM TASP R J BOTTOM, +6MM
Reason for recall
Zimmer had received complaints that reported breakage of the Persona Knee Trial Articular Surface Provisionals (TASPs). This is a retrospective recall which covers Zimmer's corrective actions taken earlier this year concerning the TASPs.
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-2297-2014. 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.