Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
This recall has been terminated (originally issued December 17, 2019).
- Company
- Arthrex, Inc.
- Recall Initiated
- December 17, 2019
- Terminated
- August 31, 2023
- Recall Number
- Z-0919-2020
- Quantity
- 47
- Firm Location
- Naples, FL
- Official Source
- View on FDA website ↗
Reason for Recall
There is a potential for blockage of the Hub Attachment Tube.
Distribution
Nationwide in US; no distribution OUS.
Lot / Code Info
Batch/Lot 051838
Root Cause
Process control
Action Taken
Consignees were notified via e-mail with recall letter dated 12/17/2019. The letter identified affected product, reason for recall, and instructed consignee to immediately discontinue use, sale, and distribution of the product as well instructions for handling of affected product.
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