Drug recall
T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be…
FDA recall event 87906 · Class II · Flower Orthopedics Corporation
Key facts
| Event ID | 87906 |
|---|---|
| Recall numbers | Z-1698-2021 |
| Recalling firm | Flower Orthopedics Corporation |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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 |
| Initiation date | Apr 15, 2021 |
| Report date | Jun 9, 2021 |
| Termination date | Nov 12, 2021 |
| City | Horsham |
| State | PA |
| Country | United States |
| FEI number | 3009996260 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: