Stop using nowMedical device recall · FDA · Published June 28, 2019
Intellijoint Workstation G2 Recall: Fire Risk from Overheating Battery
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.
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.
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📍Recalling firmIntellijoint Surgical, Inc.60 Bathurst Dr Unit 1 · Waterloo, Canada
“Intellijoint Workstation G2 Recall: Fire Risk from Overheating Battery.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67547-intellijoint-workstation-g2-recall-fire-risk-from-overheating-battery. Based on FDA recall #Z-2228-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2228-2019%22&limit=1).
Intellijoint Surgical, Inc. recalled the Workstation, G2, Configured (P/N 000-0241) due to a fire safety risk from an overheating Apple battery, according to the FDA on June 28, 2019.
Apple determined that the battery in a limited number of older generation 15-inch MacBook Pro Units may overheat and pose a fire safety risk. The affected units are part of the Intellijoint HIP System.
Context
GovInfoNow's records show Intellijoint Surgical, Inc. has two other recalls on record since February 11, 2020. On August 28, 2026, Intellijoint recalled the Navigation System Workstation G2 due to fire risk from an Apple battery. On February 11, 2020, Intellijoint recalled navigation software for incorrect knee surgery depth calculations. Other recent recalls of similar products include Nerivio Infinity Software Version 4.1.2.0 Recall (March 23, 2026) and Tobii Dynavox TD Navio Maxi/Midi Speech Device Recalls (July 8, 2026).
How to tell if you have this one
Check for the product model 'Workstation, G2, Configured' with serial numbers starting with C02R4 (e.g., C02R4A0ZG8WN). The recall includes units sold between 2019 and 2020 with these specific serial numbers.
Brand
Intellijoint
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Immediately stop using the affected MacBook Pro units as they pose a fire risk.
Where it went and when
Where it was distributed
Distributed in 5 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “IL, CA, NY, TX, RI, Australia” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Illinois, New York, Rhode Island, Texas.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2228-2019 (June 28, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2228-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.