NDI P7 Position Sensor — Class II medical device recall Z-2048-2017
Terminated recall by Orthosoft, Inc. dba Zimmer CAS, reported 2017-05-17, distributed in FL, IN, KS, LA, MS, NJ, WA, WI. Zimmer CAS voluntarily conducted a retrospective recall on specific P7 Position Sensors (Cameras), installed o
| Recall number | Z-2048-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Orthosoft, Inc. dba Zimmer CAS, Montreal, N/A, Canada |
| Recall initiated | 2009-06-09 |
| Classified | 2017-05-08 |
| Reported by FDA | 2017-05-17 |
| Terminated | 2017-05-09 |
| Distributed | FL, IN, KS, LA, MS, NJ, WA, WI |
| Countries outside the US | AT, AU, CA, CH, CZ, DE, GB, NL, SG |
| Quantity | 34 |
| Model numbers | 521.035 |
Product
NDI P7 Position Sensor, Stereotaxic Instrument
Reason for recall
Zimmer CAS voluntarily conducted a retrospective recall on specific P7 Position Sensors (Cameras), installed on Sesamoid and Sesamoid Plasty CAS workstations due to a series of these components determined to be affected with a manufacturing issue whereby they may potentially stop functioning during usage.
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-2048-2017. 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.