Stryker 1) Asnis III Cannulated Screw REF 604640 4 — Class II medical device recall Z-2099-2013
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2013-09-04, distributed nationwide. Stryker received a report that the length of the cannulated screw asnis III, article # 604640 Lot R11482, was
| Recall number | Z-2099-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2013-07-08 |
| Classified | 2013-08-27 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2015-03-31 |
| Distributed | Nationwide (US) |
| Quantity | 23 units |
| Lot numbers | R09071, R11428 |
| Model numbers | 13.5MM, 14MM, 4.0X40MMTL, 4.0X42MMTL, 604640, 604642S |
Product
Stryker 1) Asnis III Cannulated Screw REF 604640 4.0x40mm TL 13.5mm 2) Asnis III Cannulated Screw REF 604642S 4.0x42mm TL 14mm, sterile Product Usage: The Asnis III Cannulated Screw System is intended for fracture fixation of small and long bones and of the pelvis. The system is not intended for spinal use.
Reason for recall
Stryker received a report that the length of the cannulated screw asnis III, article # 604640 Lot R11482, was incorrect.
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-2099-2013. 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.