Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to… — Class II medical device recall Z-0410-2014
Terminated recall by Synthes USA HQ, Inc., reported 2013-12-04, distributed nationwide. Complaints were received of inconsistencies in the expiration dates shown on the packaging of the Vertebroplas
| Recall number | Z-0410-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synthes USA HQ, Inc., West Chester, PA, United States |
| Recall initiated | 2013-07-30 |
| Classified | 2013-11-26 |
| Reported by FDA | 2013-12-04 |
| Terminated | 2015-04-16 |
| Distributed | Nationwide (US) |
| Quantity | 40 |
| Lot numbers | AJM838X |
| Model numbers | 03.702.218S |
Product
Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement into vertebral bodies during Vertebroplasty procedure.
Reason for recall
Complaints were received of inconsistencies in the expiration dates shown on the packaging of the Vertebroplasty Needle Kit 10g Diamond Tip device.
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-0410-2014. 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.