Persona The Personalized Knee System 2 — Class II medical device recall Z-2737-2014
Terminated recall by Zimmer, Inc., reported 2014-10-08, distributed nationwide. The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use of the screw in cortical bone, an
| Recall number | Z-2737-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-09-09 |
| Classified | 2014-09-30 |
| Reported by FDA | 2014-10-08 |
| Terminated | 2015-05-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, DE, JP, SG |
| Quantity | 16,380 units |
| Lot numbers | 62155015, 62165014, 62165015, 62165016, 62165017, 62165018, 62182742, 62182743, 62188282, 62188283, 62191355, 62191361, 62191366, 62191372, 62210290, 62210291, 62227943, 62230668, 62230669, 62230670, 62230671, 62230672, 62230673, 62230674, 62230675, 62230676, 62255591, 62255592, 62255593, 62255594, 62255595, 62255596, 62255597, 62255598, 62283576, 62283577, 62283578, 62288220, 62288221, 62288222 and 47 more |
Product
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation, single use.
Reason for recall
The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use of the screw in cortical bone, and corresponding stripping of the 2.5mm Persona Hex Driver.
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-2737-2014. 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.