FPS 35mm x 3.5 mm non-locking screw
FDA Recall Z-2835-2016 · Posted None
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Recalling FirmOrtho Solutions Inc
Recall StatusTerminated
Product CodeHWC
Date Initiated2016-07-21
Date Terminated2016-10-12
Product Quantity15
Reason for Recall
Mislabeling of a single batch of FPS 3.5 x 35 mm Locking Screw as being Non-Locking Screws.
Firm Action
Ortho Solutions sent a "Field Safety Notice" letter dated July 21, 2016 to their affected customers.
The letter identify the Solutions Business Development Manager will contact the customer to arrange for the isolation and removal of the unused product from their inventory. Replacement product will be provided. The customer was advised to passed on the "Field Safety Notice" to all who need to be aware within their organization and to any organization to which their have further distributed or transferred the affected screw. Upon removal of the affected device, customers are asked to please sign and return the "Field Safety Corrective Action Declaration Form", by which to confirm they have received the "Field Safety Notice" and that they declare that the required recall has been completed at their hospital. For further questions, call (201) 258-7305.
Root Cause
Labeling mix-ups
Distribution Pattern
US 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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