Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1102-2023 — WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS 10-702-095115-0 Short 10-702-115150-0 Medium 10-702-140200 Long 10-702-190300-0

U.S. FDA — Device Enforcement · United States · 2023-01-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1102-2023
Date of alert
2023-01-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Wishbone Medical, Inc.
Product category
device
Product type
Devices
Reported risk: Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts due to the collar release pin backing out. This may lead to a delay in correction.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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