Waterloo, N/A, Canada
Intellijoint Surgical, Inc. recalls
3 recalls recorded since 2018, most recently on 28 August 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls3
Ongoing (FDA)1
Terminated or completed2
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 28 August 2026
- Reason
- A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat and pose a fire safety risk.
- Distribution
- Worldwide - US Nationwide distribution in the states of CA, TX, MS, NJ and the countries of Singapore, Spain.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0119-2027
- Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249
Terminated Class II Medical devices
- Recall started
- 11 February 2020
- Terminated
- 10 June 2020
- Reason
- During total knee arthroplasty (TKA), the software may incorrectly calculate femur resection depth.
- Distribution
- Worldwide distribution - US Nationwide distribution in the states of NY and CT. Country of Canada.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1559-2020
- Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage: The Intellijoint Navigation System is a computer-controlled, optical localizer intended to provide intra-operative measurements t
Terminated Class II Medical devices
- Recall started
- 28 June 2019
- Terminated
- 16 September 2020
- Reason
- Apple has determined that, in a limited number of older generation 15-inch MacBook Pro Units, the battery may overheat and pose a fire safety risk. To date, Intellijoint has distributed, 15-inch MacBook Pros which are the Workstation component (affected P/N 000-0241) in the Intellijoint HIP System.
- Distribution
- IL, CA, NY, TX, RI, Australia
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2228-2019
- Workstation, G2, Configured (P/N 000-0241)
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.