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Recall Observatory FDA recall evidence

Device product

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

Z-0212-2024

October 04, 2023

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 93161
Status
Ongoing
Classification
Class II
Quantity
499 beds
Official record key
device-enforcement:Z-0212-2024

Official wording

Reason: 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.

Code information: UDI/DI 00887761966925, all serial numbers

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.