Med-Mizer recalls AC-powered PR1000 Pivot Rehab Beds (2010-2014) due to wire pinching when pivoting left, requiring bed transfer until fixed.
Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made
Med-Mizer is recalling AC-powered PR1000 Pivot Rehab Beds made between December 2010 and December 2014 because wire pinching can occur when pivoting to the extreme left. This may require transferring a resident to another bed until repairs are made.
When the bed is pivoted to the extreme left, wires or cables can become pinched. This could cause a failure that requires transferring a resident to a different bed until repairs are completed.
Residents using Med-Mizer PR1000 Pivot Rehab Beds built between December 2010 and December 2014 are affected. Those with beds that pivot to the extreme left are most at risk.
Check for PR1000 Pivot Rehab Beds with serial numbers from PR10001 (built Dec 2010) to PR10255 (built Dec 2014). The beds are AC-powered adjustable beds used in rehab settings.
Look for the serial number on the bed, which should be between PR10001 and PR10255 for affected models.
Reach out to Med-Mizer directly for assistance with the recall process.
The bed may have wires or cables pinched when pivoted to the extreme left, causing a failure that requires transferring a resident to another bed until repairs are made.
Check the bed's serial number to see if it falls within the affected range (PR10001 to PR10255). Contact Med-Mizer for further instructions.
The recall record does not specify a fix or remedy, but the manufacturer will likely address the issue once the bed is identified.
We’ve drafted a message you can send Med-Mizer to request your refund or repair — edit it as you like.
Subject: Recall Z-3183-2018 — Med-Mizer Med-Mizer Hello, I own a Med-Mizer that is covered by recall Z-3183-2018 from Med-Mizer. 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.
