Recall StatusOpen, Classified
Date Initiated2026-06-10
Product Quantity62 units
Reason for Recall
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Firm Action
On June 8, 2026, Orthofix issued a Urgent Medical Device Recall Notification, via E.Mail. Orthofix asked consignees to take the following actions:
1.Discontinue use of the affected product lots immediately.
2.Immediately examine your inventory and quarantine any affected product and return them to Orthofix.
3. Complete the attached response form and return it to Orthofix.
4. This notice should be shared with all relevant personnel within your organization and forwarded to any other organization or facility where potentially affected devices may have been transferred.
Root Cause
Process change control
Distribution Pattern
US: AZ CA CO CT FL GA ID IL IN LA MD MI MO MS MT NC NY OH OR SC SD TX UT VA WA WI
OUS: None
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.