PILLAR SA Ti, STERILE, 37mm (W) x 28mm (D) x 18mm (H), 20-degrees, REF: 82-3713SP
This recall is currently active, issued September 11, 2025. It was issued by Orthofix U.S. Llc.
- Company
- Orthofix U.S. Llc
- Recall Initiated
- June 24, 2025
- Posted
- September 11, 2025
- Recall Number
- Z-2555-2025
- Quantity
- 3
- Firm Location
- Lewisville, TX
- Official Source
- View on FDA website ↗
Reason for Recall
A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap information box. The 37 mm width on the front labels is correct.
Distribution
US Nationwide distribution in the states of CO, CA.
Lot / Code Info
UDI-DI: 18257200161010, Lots: 001, 002, and 003
Root Cause
Labeling design
Action Taken
On 6/24/2025, recall notes were emailed to customers who were asked to do the following: 1) Examine your inventory and quarantine any affected product. 2) If implanted, healthcare Providers should determine whether it is necessary to inform the patient, based on clinical judgment and individual circumstances. 3) 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. 4) Complete and return the response form to the firm. Should you have any questions regarding this matter, please contact the firm at madison.ebel@seaspine.com