JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty
FDA Recall Z-0993-2018 · Posted None
Recalling FirmZimmer Biomet, Inc.
Recall StatusTerminated
Product CodeLZO
Date Initiated2017-06-30
Date Terminated2018-04-13
Product Quantity50
Reason for Recall
For soft tissue fixation
Firm Action
On June 2, 2017 an URGENT Medical Recall Letter was issued to customers regarding affected product(s). The letter requests customers to review the content and notify affected personnel of the recall. Assist the sales representative in quarantining affected product, which will be removed and returned to recalling firm and then replaced. All customers who may have received product from distributors are to be notified. Questions or concerns can be directed to 1-574-372-4847.
Root Cause
Packaging process control
Distribution Pattern
US in the state of Texas
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.