Baxter Healthcare Corporation: Medical Device Recall in 2023 - (Recall #: Z-0212-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: October 4, 2023

Date Posted: November 8, 2023

Recall Number: Z-0212-2024

Event ID: 93161

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.

Status: Ongoing

Product Quantity: 499 beds

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

Voluntary or Mandated:

Voluntary: Firm initiated