Pathfinder NXT Fixed Percutaneous Rod Holder — Class II medical device recall Z-1980-2012
Terminated recall by Zimmer, Inc., reported 2012-07-18, distributed nationwide. Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because complaints have been received that t
| Recall number | Z-1980-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2012-06-05 |
| Classified | 2012-07-10 |
| Reported by FDA | 2012-07-18 |
| Terminated | 2014-09-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CH, ES, FR, GB, IT |
| Quantity | 249 |
| Reason classes | packaging, device malfunction |
| Model numbers | 3573-1 |
Product
Pathfinder NXT Fixed Percutaneous Rod Holder, Part numbers 3573-1 (angle handle) , Stainless Steel / Silicone Rubber, Rx only, non sterile. Product Usage: The rod is held by the instrument for inserting and guiding into the screw heads via percutaneous delivery during minimally invasive surgery to fuse the spine. Per the surgical technique (Ll554 Pathfinder NXT Surgical Technique);
Reason for recall
Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because complaints have been received that the rod holder tip may crack or break when the rod is manipulated during surgery.
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-1980-2012. 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.