# FDA recall Z-0212-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2023-10-04.

## Product

HILLROM PROGRESSA+ BED, Product Codes:  P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, P7501A000052, P7501A000053, P7501A000054, P7501A000055, P7501A001851, P7501A001972, P7501A001973, and P7501A001974

## Reason for recall

Progressa+ beds have the potential for static buildup from the casters and/or power drive. This static electricity could be passed to the operator through the transport handle during transport, resulting in a mild static electric shock.

## Distribution

US Nationwide Distribution in the states of:  CA, FL, IN, MA, NY, OH, TX, VA

## Key facts

- **Recall number:** Z-0212-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-04
- **Report date:** 2023-11-08

- **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-0212-2024

## Citation

> AI Analytics. FDA recall Z-0212-2024. Retrieved 2026-09-09 from https://api.ai-analytics.org/recall/Z-0212-2024. Source: US FDA. Licensed CC0.

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