RecallRadar

FDA Device recall Z-0119-2027

Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241

On 2026-10-14 the FDA classified a Class II recall of Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241 by Intellijoint Surgical, citing A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to a….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0119-2027
ClassificationClass II
Statusongoing
Initiated2026-08-28
Published2026-10-14
Last updated2026-10-21 05:30 UTC
CompanyIntellijoint Surgical
DistributionUS

Product

Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249

Reason

A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat and pose a fire safety risk.

Identifiers

code_info
REF/UDI-DI/MacBook Serial Numbers: 000-0241/00628184002414/C02RP36YG8WP, C02QPCF5G8WN 000-0250/00628184002506/C02RF44TG…REF/UDI-DI/MacBook Serial Numbers: 000-0241/00628184002414/C02RP36YG8WP, C02QPCF5G8WN 000-0250/00628184002506/C02RF44TG8WN, C02QW25RG8WL, C02QH355G8WM, C02S22N9G8WP; 000-0249/00628184002490/C02RQ3FUG8WN, C02R4451G8WN

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-21 05:30 UTC. Current status: ongoing.

Other recalls by Intellijoint Surgical

All Intellijoint Surgical recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0119-2027%22

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