Getinge recalls Nimbus 4 and Nimbus Professional alternating-pressure bed mattress overlays due to potential for abnormal mattress inflation. Affected models include 650001ADV, 650001DAR, and others listed in the recall notice.
There is a potential for abnormal inflation of the mattress.
Getinge is recalling Nimbus 4 and Nimbus Professional alternating-pressure bed mattress overlays because they may inflate abnormally. This could cause the mattress to become too firm or too soft, potentially leading to discomfort or injury during use.
The mattress overlay may inflate abnormally, causing it to become too firm or too soft. This could lead to discomfort or injury if the mattress does not maintain proper support during patient care.
Patients and healthcare workers using the Nimbus 4 or Nimbus Professional bed mattress overlays are most at risk. The recall affects specific model numbers sold in China.
Check for model numbers: 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, or 651201P. These models were sold in China by Getinge (Suzhou) Co Ltd.
Look for model numbers listed in the recall notice: 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, or 651201P.
The affected models are 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, and 651201P.
Check the model numbers on your Nimbus 4 or Nimbus Professional bed mattress overlay. The affected models were sold in China by Getinge (Suzhou) Co Ltd.
The recall notice does not specify a remedy, so contact Getinge (Suzhou) Co Ltd directly for further instructions.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-1788-2021 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-1788-2021 from Getinge. 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.
