HILLROM PROGRESSA+ beds with specific product codes may cause mild static shocks during transport due to caster static buildup. Affected units include models P7501A000016 to P7501A001974. No action needed for most users.
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.
HILLROM PROGRESSA+ beds with certain product codes may cause mild static shocks when moved. This happens because static electricity builds up from the casters and can be transferred to the user through the transport handle during transport. The risk is low and only affects specific bed models.
Static electricity builds up in the bed's casters during movement. When the transport handle is used, this static can transfer to the user, causing a mild electric shock. The shock is not severe but may be uncomfortable.
Users of HILLROM PROGRESSA+ beds with product codes P7501A000016 through P7501A001974 are most at risk. This includes hospital and home users who transport the beds.
Check your bed's product code on the label or documentation. Affected models include P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, and other codes listed in the recall notice.
Look for the product code on the bed's label or documentation to confirm if it's affected.
No, the recall involves a mild static shock risk during transport, which is not serious.
No action is needed for most users; the recall only applies to specific product codes.
Check the product code on the bed's label or documentation. Affected models include P7501A000016 through P7501A001974.
We’ve drafted a message you can send HILLROM to request your refund or repair — edit it as you like.
Subject: Recall Z-0212-2024 — HILLROM HILLROM Hello, I own a HILLROM that is covered by recall Z-0212-2024 from HILLROM. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
