🔍 RecallPedia

Nimbus 4 and Nimbus Professional Alternating-pressure bed mattress overlay system

Class I - Dangerous
🏥 Medical Devices Recalled: April 15, 2021 Getinge (Suzhou) Co Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Model Numbers: 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, 651201P Product Code: 47478 (GMDN nomenclature code)
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Getinge (Suzhou) Co Ltd
Reason for Recall:
There is a potential for abnormal inflation of the mattress.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Nimbus 4 and Nimbus Professional Alternating-pressure bed mattress overlay system

Product Codes/Lot Numbers:

Model Numbers: 650001ADV, 650001DAR, 650001P, 650201DAR, 651001, 651001ADV, 651001DAR, 651001DARW, 651001P, 651201DAR, 651201P Product Code: 47478 (GMDN nomenclature code)

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1788-2021