# FDA recall Z-1817-2022

> **Baxter Healthcare Corporation** · Class III · device recall initiated 2022-09-02.

## 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.

## Reason for recall

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

## Distribution

US Nationwide Distribution and government/military distribution.

## Key facts

- **Recall number:** Z-1817-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-02
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1817-2022

## Citation

> AI Analytics. FDA recall Z-1817-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1817-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*