Stryker Corporation Recall: Stryker CinchLock Flex Knotless Anchor with Inserter and Sutur
Stryker Corporation Recall: Stryker CinchLock Flex Knotless Anchor with Inserter and Sutur is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Stryker Corporation; Product: Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197; R
| Recalling firm | Stryker Corporation |
|---|---|
| Product | Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197 |
| Reason for recall | Increase in complaints concerning "pullwire" breakage that may result in the broken pullwire remaining in the anchor implant body after deployment. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide - US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Michigan, Minnesota, Mississippi, Missouri, Monta |
| Recall initiated | 20250129 |
| Recall number | Z-1328-2025 |
| Category | device |
| State | CA |
| Country | United States |
$29/mo
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