FDA recall Z-0212-2024

Baxter Healthcare Corporation · Class II · device

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

Status
Ongoing
Initiation date
2023-10-04
Report date
2023-11-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0212-2024