RegWardenFDA facility compliance records
Recall

Class II — Intellijoint Surgical, Inc.

Recalling firmIntellijoint Surgical Inc.
Registered facilityIntellijoint Surgical Inc. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonApple 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.
ProductWorkstation, G2, Configured (P/N 000-0241)
Quantity23 units
DistributionIL, CA, NY, TX, RI, Australia
Initiated2019-06-28
Classified2019-08-08
Terminated2020-09-16
Recall numberZ-2228-2019
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Intellijoint Surgical, Inc. (Z-2228-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83299/

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