FDA Medical Device Recalls (openFDA)
Stryker Corporation: Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462
- Recall number
- Z-2645-2023
- Recalling firm
- Stryker Corporation
- Product
- Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462
- Status
- Open, Classified
- Initiated
- 2023-08-23
- Posted
- 2023-09-28
- Terminated
- not on file
- Reason
- Expired Product distributed
- Root cause
- Unknown/Undetermined by firm
- Action
- On August 23, 2023, Stryker issued an "Urgent Medical Device Recall Notification" to affected consignees via . Stryker asked consignees to take the following actions: Actions needed: 1. Inform individuals within your organization who need to be aware of this device recall. 2. Check all inventory to determine if any devices from the affected product list are located at your facility. Response is required by September 30, 2023. 3. If affected product is found, quarantine and discontinue use of the recalled devices. Please complete the response form on Appendix A of this notice and return devices back to Stryker Endoscopy. 4. If no product is found, complete acknowledgement form and return it back to Stryker.
- Quantity
- 96 units
- Distribution
- US Nationwide distribution in the states of NY, NC, GA, TN, KY, IL, UT, AZ, NM, CA.
- Lot, serial or model codes
- Lot # 19175AE2
- 510(k) numbers
- ["K131769"]
- PMA numbers
- not on file
- Product code
- MBI
- Firm FEI
- 2936485
- Firm city
- San Jose
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28