T25 Cannulated Screwdrivers — Class II medical device recall Z-1698-2021
Terminated recall by Flower Orthopedics Corporation, reported 2021-06-09, distributed nationwide. Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time an
| Recall number | Z-1698-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Flower Orthopedics Corporation, Horsham, PA, United States |
| Recall initiated | 2021-04-15 |
| Classified | 2021-06-01 |
| Reported by FDA | 2021-06-09 |
| Terminated | 2021-11-12 |
| Distributed | Nationwide (US) |
| Quantity | 47 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00840118110853 |
| Lot numbers | 1711220035, 1802220005, 1802220008, 1810220041, 2003320898 |
Product
T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm Product Code: GWK 300
Reason for recall
Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages
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-1698-2021. 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.