Z-0212-2024 Class II Ongoing
FDA device recall Z-0212-2024 was initiated by Baxter Healthcare Corporation on Oct 4, 2023 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 499 beds.
Recall details
- Product Type
- Devices
- Report Date
- Nov 8, 2023
- Initiation Date
- Oct 4, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 499 beds
Product description
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 pattern
US Nationwide Distribution in the states of: CA, FL, IN, MA, NY, OH, TX, VA
Code information
UDI/DI 00887761966925, all serial numbers
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0212-2024
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026