Workstation — Class II medical device recall Z-2228-2019
Terminated recall by Intellijoint Surgical, Inc., reported 2019-08-14, distributed in CA, IL, NY, RI, TX. Apple has determined that, in a limited number of older generation 15-inch MacBook Pro Units, the battery may
| Recall number | Z-2228-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intellijoint Surgical, Inc., Waterloo, N/A, Canada |
| Recall initiated | 2019-06-28 |
| Classified | 2019-08-08 |
| Reported by FDA | 2019-08-14 |
| Terminated | 2020-09-16 |
| Distributed | CA, IL, NY, RI, TX |
| Countries outside the US | AU |
| Quantity | 23 units |
| Reason classes | device malfunction |
| Serial numbers | C02R4A0ZG8WN, C02R4CTHG8WN, C02R4CTLG8WN, C02R4CUZG8WN, C02R4CV6G8WN, C02R4CVYG8WN, C02R4CWZG8WN |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2228-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.