Skip to content
Recall Observatory FDA recall evidence

Device product

Starling Monitor, Product code CMMST5 and Starling Monitor SV, Product code CMM-ST5 (same products); and accessories/spare parts Starling Battery Pack, Product Code CMABATT; and Starling Patient Cable, Product code CMASC10.

Z-1817-2022

September 02, 2022

Class III

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 90809
Status
Ongoing
Classification
Class III
Quantity
9,671 units
Official record key
device-enforcement:Z-1817-2022

Official wording

Reason: Labeling has incorrect or incomplete Unique Device Identification (UDI) information; and the barcodes are not compliant with GS-1 standards.

Code information: All serial numbers after 6/2016. Product code CMMST5 - Incorrect UDI-DI: 7290013030269; correct UDI-DI: 07290013030269. Product code CMM-ST5 - Incorrect UDI-DI: 7290013030030; correct UDI-DI: 07290013030030. Product code CMABATT - Incorrect UDI-DI: 7290013030160; correct UDI-DI: 07290013030160. Product code CMASC10 - Incorrect UDI-DI: 7290013030054; correct UDI-DI: 07290013030054.

Distribution pattern: US Nationwide Distribution and government/military distribution.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Labeling has incorrect or incomplete