Nextremity Solutions recalls
Every recall we track for Nextremity Solutions — 15 in all, from 2019–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Nextremity Solutions peaked in 2022 (7); 15 since 2017.
All FDA recall records for Nextremity Solutions 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 | 5 | 0 | 5 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 2 | 4 | 1 | 7 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Nextremity Solutions recalls
What to do if you have a recalled Nextremity Solutions 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 Nextremity Solutions recalls
7 shown- Lower riskMedical device
Nextremity Solutions recalls Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut SKU: NX-3532K-SC Orthopedic surgical instrument
Nextremity recalls specific orthopedic surgical instruments due to oversized driver causing surgery delays. Affected units have SKU NX-3532K-SC and lot number 1681250:17B.
Nextremity SolutionsFeb 10, 2022 - UnratedMedical device
Nextremity Solutions recalls Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital
Nextremity Solutions recalls its Nextra CH Cannulated Hammertoe Mini Instrument Kit for potential surgical complications. The device may deform the implant locking mechanism during insertion, leading to delays or revision surgery.
Nextremity SolutionsJan 13, 2022 - Lower riskMedical device
Nextremity Solutions recalls InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product Usage: Intended as a three-part construct
Nextremity Solutions recalls InCore Lapidus 28mm Left kit (part IC-LAP-28L) due to potential undersized drill bushing that may prevent surgical procedure completion.
Nextremity SolutionsMar 26, 2021 - Lower riskMedical device
Nextremity Solutions recalls Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra
Nextremity recalls Nextra Hammertoe Correction System-4.5MM Middle, : Oversized proximal driver may cause difficulty connecting with implant. Affected units have lot number 168117318B and UDI 00817701020011.
NextremityFeb 12, 2020 - Lower riskMedical device
Nextremity Solutions recalls Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot
Nextremity Solutions recalls Stratum Lapidus Plate (Part No. STRM-LAP-SMR) due to incorrect plate type. This could cause improper bone fixation. Affected units have UDI 00817701025467.
Nextremity SolutionsDec 16, 2019 - Lower riskMedical device
Nextremity Solutions recalls Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST
Nextremity Solutions recalls Stratum MDS Screw 3.5x50mm ST (part number STRM-MDS-3550ST) due to components being 2mm shorter than labeled. Affected units include lot M1268 with UDI 00817701023173.
Nextremity SolutionsNov 11, 2019 - Lower riskMedical device
Nextremity Solutions recalls Stratum Foot Plating System-NL LP Screw 3.5x50mm ST, sterile. Catalog Number: STRM-NL-3550ST - Product Usage: The
Nextremity Solutions recalls Stratum Foot Plating System NL LP Screw 3.5x50mm ST (lot M1151) due to possible incorrect screw type and length. Affected users should check their product details.
Nextremity SolutionsOct 9, 2019
Nextremity Solutions recall questions
How many recalls has Nextremity Solutions had?
15 recalls from Nextremity Solutions are on record with U.S. safety agencies, from 2019–2022.
What is the most recent Nextremity Solutions recall?
Nextremity Solutions recalls Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut SKU: NX-3532K-SC Orthopedic surgical instrument, dated Feb 10, 2022. Every Nextremity Solutions recall is listed on this page, newest first.
Why are Nextremity Solutions products recalled?
The most common reasons on record: Components 2mm shorter than indicated on the package label (3).
What should I do if I have a recalled Nextremity Solutions 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 Nextremity Solutions 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.