Arthrex, Inc. Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Brand
Arthrex, Inc.
Lot Codes / Batch Numbers
Batch/Lot 051838
Products Sold
Batch/Lot 051838
Arthrex, Inc. is recalling Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting due to There is a potential for blockage of the Hub Attachment Tube.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for blockage of the Hub Attachment Tube.
Recommended Action
Per FDA guidance
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.
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 noticePage updated: Jan 10, 2026