Hill-Rom recalls Affinity Four Birthing Beds (models P3700B-E) with damaged latch mechanism that could cause improper engagement and fall injuries during labor/delivery. Affected units have specific serial numbers listed in the recall notice.
Latch mechanism on the Lift-Off foot section of the Affinity Four Birthing Bed is damaged, it could potentially cause the installed foot section to be improperly engaged onto the bed, could result in injury to the user due to a fall.
Hill-Rom is recalling Affinity Four Birthing Beds used in labor and delivery settings because a damaged latch mechanism could cause the foot section to become improperly engaged, potentially leading to falls and injuries. This recall affects specific models and serial numbers.
The latch mechanism on the Lift-Off foot section can become damaged, causing the foot section to be improperly engaged with the bed. This could lead to the user falling if the foot section becomes disengaged during use.
Women in labor and delivery settings who use the Affinity Four Birthing Bed as a birthing bed. The risk is highest for users who may not have the bed properly secured.
Check if your Affinity Four Birthing Bed has model numbers P3700B, P3700C, P3700D, or P3700E and the listed serial numbers in the recall notice. These beds are used in LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) settings.
Inspect the Lift-Off foot section latch for damage or improper engagement.
If the latch is damaged, stop using the bed immediately to prevent falls.
Models P3700B, P3700C, P3700D, and P3700E.
Check the serial numbers listed in the recall notice; affected units have specific US and OUS serial numbers provided in the record.
Inspect the latch mechanism on the Lift-Off foot section. If damaged, stop using the bed immediately to prevent falls.
We’ve drafted a message you can send Hill-Rom to request your refund or repair — edit it as you like.
Subject: Recall Z-2156-2021 — Hill-Rom Hill-Rom Hello, I own a Hill-Rom that is covered by recall Z-2156-2021 from Hill-Rom. 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.
