Drug recall
CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of…
FDA recall event 87717 · Class II · Smith & Nephew, Inc.
Key facts
| Event ID | 87717 |
|---|---|
| Recall numbers | Z-1510-2021 |
| Recalling firm | Smith & Nephew, Inc. |
| Product type | Devices |
| Products | CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of soft tissue grafts in anterior cruciate ligament reconstruction, Part Number… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw |
| Initiation date | Apr 8, 2021 |
| Report date | May 5, 2021 |
| Termination date | Jun 22, 2022 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 3003604053 |
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: