Wright Medical Technology, Inc. stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
Brand
Wright Medical Technology, Inc.
Lot Codes / Batch Numbers
UDI/DI 00889797004008, Lot Numbers: 2656950, 2762126, 2796094
Products Sold
UDI/DI 00889797004008, Lot Numbers: 2656950, 2762126, 2796094
Wright Medical Technology, Inc. is recalling stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty due to Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were foun. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.
Recommended Action
Per FDA guidance
Stryker issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 03/06/2024 via email. The notice explained the issue, potential risk, and requested the consignee isolate/quarantine the affected product pending return of the device. If the affected product was further distributed, please notify the applicable parties at once about this recall. This notification letter may be copied and distributed. a. If possible, inform Stryker if any of the subject devices have been distributed to other organizations, including contact details so that we can inform the recipients appropriately. b. If you are a distributor, note that you are responsible for notifying your affected customers. For questions or concerns, please contact memphis.fieldaction@stryker.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
NE, TX
Page updated: Jan 10, 2026