Intellijoint Surgical, Inc. recalls
Every recall we track for Intellijoint Surgical, Inc. — 3 in all, from 2019–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Intellijoint Surgical, 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 | 1 | 0 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 1 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
What to do if you have a recalled Intellijoint Surgical, 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 Intellijoint Surgical, Inc. recalls
3 shown- Use cautionMedical device
Intellijoint Surgical, Inc. recalls Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250;
Intellijoint Navigation System Workstation G2 (REF: 000-0241) may overheat due to Apple battery recall, posing fire risk. Affected units include specific REF and MacBook serial numbers. Contact manufacturer for remedy.
IntellijointAug 28, 2026 - UnratedMedical device
Intellijoint Surgical, Inc. recalls Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage: The Intellijoint Navigation
Intellijoint recalls its Navigation System software (V1.2.0/V1.2.1) due to potential incorrect femur depth calculations during knee surgery. Affected devices may require correction to prevent surgical errors.
IntellijointFeb 11, 2020 - Stop using nowMedical device
Intellijoint Surgical, Inc. recalls Workstation, G2, Configured (P/N 000-0241)
Intellijoint recalls specific 15-inch MacBook Pro units (P/N 000-0241) due to potential battery overheating and fire risk. Affected units have unique Apple serial numbers listed in the recall notice.
IntellijointJun 28, 2019
Intellijoint Surgical, Inc. recall questions
How many recalls has Intellijoint Surgical, Inc. had?
3 recalls from Intellijoint Surgical, Inc. are on record with U.S. safety agencies, from 2019–2026.
What is the most recent Intellijoint Surgical, Inc. recall?
Intellijoint Surgical, Inc. recalls Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250;, dated Aug 28, 2026. Every Intellijoint Surgical, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Intellijoint Surgical, 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 Intellijoint Surgical, 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.