Hill-Rom Progressa Bed System
Reported: November 23, 2022 Initiated: October 18, 2022 #Z-0231-2023
Product Description
Hill-Rom Progressa Bed System
Reason for Recall
The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 248 beds (Updated)
- Distribution
- Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, HI, IN, LA, MA, MO, NC, NM, NV, NY, OK, OR, PA, SC. TN, TX, WA, and WI. (UPDATED: States of PA and SC and there was government distribution.) There was no military distribution. Foreign distribution was made to Canada, Qatar, Singapore, and UAE. UPDATE: Saudi Arabia now included.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Hill-Rom Progressa Bed System. Recalled by Baxter Healthcare Corporation. Units affected: 248 beds (Updated).
Why was this product recalled? ▼
The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 23, 2022. Severity: Moderate. Recall number: Z-0231-2023.
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