HILLROM PROGRESSA+ BED, Product Codes: P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, P7501A000052, P7501A000053, P7501A000054, P7501A000055, P7501A001851, P7501A001972, P7501A001973, and P7501A001974
This recall is currently active, issued November 2, 2023. It was issued by Baxter Healthcare Corporation.
- Company
- Baxter Healthcare Corporation
- Recall Initiated
- October 4, 2023
- Posted
- November 2, 2023
- Recall Number
- Z-0212-2024
- Quantity
- 499 beds
- Firm Location
- Deerfield, IL
- Official Source
- View on FDA website ↗
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
Lot / Code Info
UDI/DI 00887761966925, all serial numbers
Root Cause
Under Investigation by firm
Action Taken
Baxter issued an Urgent Medical Device Correction notice to its consignees on 10/04/2023 by USPS first class mail. The notice explained the potential problem and hazard. Baxter will be correcting this issue by installing a conductive drag chain on the Progressa+ bed frame to prevent the electrostatic charge buildup. A Baxter representative will contact your facility to schedule a device correction to add the conductive drag chain. Please note you will be receiving this correction from Baxter at no charge. All units purchased in the future will have the drag chain.