Intellijoint Navigation System and Intellijoint HIP Systems
The Intellijoint Navigation System may contain a MacBook Pro battery that can overheat and pose a fire safety risk.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Intellijoint Surgical, Inc. recalled its Intellijoint Navigation System: Workstation G2 Configured, along with the Intellijoint HIP Cart System and Intellijoint HIP, Portable System, on August 28, 2026, because the workstation may contain a 15-inch MacBook Pro battery subject to an Apple battery recall that may overheat and pose a fire safety risk. The FDA added the recall to its Enforcement Report on October 7, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Compare these product details with yours, then check the recall notice for any restrictions.
Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249
Details
- Company began the recall
- Event ID
- 99821
- Company
- Intellijoint Surgical, Inc.
- Hazard
- Device defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
