NeoSpan SuperElastic Compression Staple w/Instruments — Class II medical device recall Z-0670-2019
Terminated recall by In2bones USA, LLC, reported 2019-01-02, distributed in FL, LA, MO, NC, NJ, OH, PA, TN…. The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a
| Recall number | Z-0670-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | In2bones USA, LLC, Memphis, TN, United States |
| Recall initiated | 2018-11-14 |
| Classified | 2018-12-22 |
| Reported by FDA | 2019-01-02 |
| Terminated | 2019-05-08 |
| Distributed | FL, LA, MO, NC, NJ, OH, PA, TN, TX, VA, WI |
| Quantity | 30 units |
| Lot numbers | 9G88C0 |
| Model numbers | SN010, T50 |
Product
NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10, Part Number T50 SN010
Reason for recall
The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a 3mm drill bit instead of a 2mm drill bit.
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-0670-2019. 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.