# FDA recall Z-2228-2019

> **Intellijoint Surgical, Inc.** · Class II · device recall initiated 2019-06-28.

## Product

Workstation, G2, Configured (P/N 000-0241)

## Reason for recall

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

## Key facts

- **Recall number:** Z-2228-2019
- **Recalling firm:** Intellijoint Surgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-28
- **Report date:** 2019-08-14
- **Termination date:** 2020-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waterloo, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2228-2019

## Citation

> AI Analytics. FDA recall Z-2228-2019. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2228-2019. Source: US FDA. Licensed CC0.

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