Wishbone Medical, Inc. recalls
Every recall we track for Wishbone Medical, Inc. — 3 in all, from 2021–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Wishbone Medical, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Wishbone Medical, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Wishbone Medical, Inc. recalls
3 shown- Lower riskMedical device
Wishbone Medical, Inc. recalls WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
Wishbone Medical recalls WishFIX Growth Control Plating System (Model TEFCS28-080US) due to incorrect implant material in packaging. Affected units may have stainless steel instead of titanium.
Wishbone MedicalApr 5, 2024 - Use cautionMedical device
Wishbone Medical, Inc. recalls WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS
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.
Wishbone MedicalJan 4, 2023 - Lower riskMedical device
Wishbone Medical, Inc. recalls WishBone Medical Plate and Screw System - Screw, Fixation, Bone, Washer, Bolt Nut. Part Number: PK-SMC0635NL-TI-US,
Wishbone Medical recalls specific plate and screw systems due to engineering nonconformities. Affected products include certain part numbers and lot numbers. Consumers should check their items against the list provided.
Wishbone MedicalApr 30, 2021
Wishbone Medical, Inc. recall questions
How many recalls has Wishbone Medical, Inc. had?
3 recalls from Wishbone Medical, Inc. are on record with U.S. safety agencies, from 2021–2024.
What is the most recent Wishbone Medical, Inc. recall?
Wishbone Medical, Inc. recalls WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device., dated Apr 5, 2024. Every Wishbone Medical, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Wishbone Medical, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Wishbone Medical, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.