FDA Medical Device Recalls (openFDA)
Intellijoint Surgical, Inc.: Workstation, G2, Configured (P/N 000-0241)
- Recall number
- Z-2228-2019
- Recalling firm
- Intellijoint Surgical, Inc.
- Product
- Workstation, G2, Configured (P/N 000-0241)
- Status
- Terminated
- Initiated
- 2019-06-28
- Posted
- 2019-08-08
- Terminated
- 2020-09-16
- 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.
- Root cause
- Nonconforming Material/Component
- Action
- The firm initiated the recall by email on 06/28/2019. The letter requested the distributor locate and return the MacBooks.
- Quantity
- 23 units
- Distribution
- IL, CA, NY, TX, RI, Australia
- Lot, serial or model codes
- Apple MacBook Serial Numbers: C02R4A0ZG8WN, C02R4CTLG8WN, C02R4CVYG8WN, C02R4CTHG8WN, C02R4CUZG8WN, C02R4CV6G8WN, C02R4CWZG8WN Additional units discovered 09/18/2019: C02R4CQ5G8WN, C02R4CULG8WN, C02R4CVWG8WN, C02R4CWYG8WN, C02R4CQ6G8WN, C02R4CUPG8WN, C02R4CSSG8WN, C02R4CTQG8WN, C02R4CSZG8WN, C02R4CUSG8WN, C02R4CUXG8WN, C02R4CUQG8WN, C02R4CU0G8WN, C02R4A6PG8WN, C02R4CTMG8WN, 02R4CUNG8WN
- 510(k) numbers
- ["K172849"]
- PMA numbers
- not on file
- Product code
- OLO
- Firm FEI
- 3010822102
- Firm city
- Waterloo
- Firm state
- not on file
- Firm country
- Canada
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28