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Lower risk Medical device recall · FDA · Published April 15, 2021

Getinge Nimbus 4 Bed Mattress Overlays Risk Abnormal Inflation

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1788-2021Medical deviceGetinge ›
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Contact the company

Recalling firmGetinge (Suzhou) Co LtdNO 158 Fangzhoulu, Zhong Xin Gongyeyuanqu · Suzhou City, China
✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/62786-getinge-nimbus-4-bed-mattress-overlays-risk-abnormal-inflation.

Source Summary by GovInfoNow · govinfonow.com/recall/62786-getinge-nimbus-4-bed-mattress-overlays-risk-abnormal-inflation · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1788-2021

Cite this page

“Getinge Nimbus 4 Bed Mattress Overlays Risk Abnormal Inflation.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62786-getinge-nimbus-4-bed-mattress-overlays-risk-abnormal-inflation. Based on FDA recall #Z-1788-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1788-2021%22&limit=1).

Getinge (Suzhou) Co Ltd voluntarily recalled Nimbus 4 and Nimbus Professional Alternating-pressure bed mattress overlay systems due to potential abnormal inflation, according to the FDA on April 15, 2021.

How to tell if you have it

  • Brand: Getinge
  • Product: Nimbus 4 and Nimbus Professional Alternating-pressure bed mattress overlay system
  • Model Numbers: 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, 651201P
  • Product Code: 47478
  • Units affected: 13042

The hazard

The recall addresses the potential for abnormal inflation of the mattress.

Context

GovInfoNow's records show Baxter Healthcare issued a PRO+ 40" MRS SURFACE Mattress Recall on August 18, 2026, due to incorrect labeling risk.

How to tell if you have this one

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.

  • Brand
    Getinge
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Model Numbers

    Look for model numbers listed in the recall notice: 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, or 651201P.

How this recall unfolded

Recall timeline

FDA terminated this recall 2.6 years after the firm started it.

1. Firm started the recall: Apr 15, 202112. FDA classified it Class II: Jun 3, 202123. Published in FDA’s Enforcement Report: Jun 9, 202134. FDA terminated the recall: Nov 13, 2023420212023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-1788-2021 (April 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1788-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA