stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400; Orthopedic external fixation device intended to keep bone fragments/segments in a correct anatomical position until reliable bone consolidation is achieved
FDA Recall Z-1191-2023 · Posted 2023-03-01
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Recalling FirmStryker GmbH
Recall StatusOpen, Classified
Product CodeKTT
Date Initiated2023-02-07
Product Quantity488 units
Reason for Recall
Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a result the distal ring fixation cannot be locked between 0- 50mm of the threaded rod.
Firm Action
The firm issue an URGENT MEDICAL DEVICE RECALLL its consignees by letter on 02/07/2023. The notice explained the product and the issue and requested the following actions be taken:
1. Check inventory for affected product and remove from use
2, Sign and return the enclosed Business Reply Form by email to [email protected] to confirm receipt of this notification/documenting product disposition. Stryker will will contact you to arrange for the return of the affected device(s)
3. Spread awareness of this communication internally until all required actions have been completed within your facility.
4. Inform Stryker if any of the subject devices have been distributed to other organizations. If so, provide contact details so that Stryker can inform the recipients appropriately.
Root Cause
Process change control
Distribution Pattern
US Nationwide distribution.
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.
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