Wishbone Medical recalls Smart Correction Dual Joint Express Struts due to potential collar release pin backing out, causing delay in correction. Affected units include specific part numbers and lots.
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.
Wishbone Medical is recalling its Smart Correction Dual Joint Express Struts because the collar release pin may back out, making it difficult to adjust the device length. This could delay necessary corrections for users, particularly those requiring precise skeletal adjustments.
The collar release pin can back out, preventing users from adjusting the struts' length. This may cause delays in necessary bone correction procedures, potentially affecting treatment outcomes.
Patients using external skeleton fixation devices for bone correction, especially those needing precise adjustments. Users with the specific part numbers and lots listed are most at risk.
Check the product's part number and lot number on the device. Affected units include specific part numbers (XXS, Short, Medium, Long) and corresponding lots (1048176-1048180).
Identify the part number and lot number on the device to determine if it is affected.
The collar release pin may back out, making it difficult to adjust the struts' length, which could delay necessary bone correction.
Affected part numbers include XXS (10-702-080095-0), Short (10-702-095115-0), Medium (10-702-115150-0), and Long (10-702-140200).
Check the part number and lot number on the device. Affected units have specific part numbers and lots listed in the recall notice.
We’ve drafted a message you can send Wishbone Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1102-2023 — Wishbone Medical Wishbone Medical Hello, I own a Wishbone Medical that is covered by recall Z-1102-2023 from Wishbone Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
