Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
FDA Recall Z-1678-2022 · Posted None
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Recalling FirmOrthoPediatrics Corp
Recall StatusOpen, Classified
Product CodeKTT
Date Initiated2022-06-29
Product Quantity640 units
Reason for Recall
Manufacturing variance near transition of tip is increasing the likelihood the wire tip may fracture. The fractured tip may be retained in the patient. Retrieval attempts may be made which could result in a delay of surgery and potentially damage soft tissue and increase healing time
Firm Action
OrthoPediatrics Corp. provided Urgent Medical Device recall Letter to Distributors on 6/29/22. Letter states reason for recall, health risk and action to take:
The affected product must be returned to OrthoPediatrics Corporation. Replacement product will be provided. Please contact customer service to arrange return of the affected product.
Distributors should retrieve affected product that may be with customers. No additional
corrective actions need to be taken for product already implanted. Please complete and return the attached response acknowledgement form confirming your understanding of these instructions.
Any questions regarding this recall can be directed to Joel Batts, Senior VP of Science &
Technology, at OrthoPediatrics at [email protected] or 574-367-5396.
Root Cause
Process change control
Distribution Pattern
US Nationwide Distribution: AZ, AL, CA, FL, FL, MD, MO, NC, NY, TX Foreign: Australia
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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