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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Getinge Usa Sales Inc: MEERA Mobile Operating Tables Recalled Due to Hand Control Error and Table Stoppage

Agency Publication Date: November 14, 2024
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Summary

Getinge USA Sales Inc. has recalled 878 MEERA CL mobile operating tables because the infrared (IR) hand control may display error code "50037" and cause the table to stop moving unexpectedly. This defect affects eight different item numbers and was initiated by a voluntary firm letter in October 2024. If the operating table stops moving during a medical procedure, it can result in a procedural delay for the patient and surgical team. Consumers should contact Getinge or their healthcare provider to determine if their specific table is part of the affected serial number ranges.

Risk

The hand control can experience sporadic communication errors that stop the placement or positioning of a patient during surgery. This interruption can lead to critical procedural delays while medical staff troubleshoot the equipment or switch to manual controls.

What You Should Do

  1. Locate the serial number and item number on your MEERA CL mobile operating table to determine if it is affected by this recall.
  2. Check for Item Number 720001B0 with Serial Numbers 11399 through 11746; Item Number 720001B2 with Serial Numbers 10894 through 11128; or Item Number 720001F0 with Serial Numbers 1059 through 1091.
  3. Check for Item Number 720001F2 with Serial Numbers 579 through 639; Item Number 710001B0 with Serial Numbers 680 through 707; or Item Number 710001B2 with Serial Numbers 252 through 254.
  4. Check for Item Number 700001B0 with Serial Numbers 491 through 603; or Item Number 700001F0 with Serial Number 9.
  5. If your device matches the affected item and serial numbers, contact your healthcare provider or Getinge USA Sales Inc. at 1 Geoffrey Way, Wayne, New Jersey, 07470-2035 for technical support and instructions.
  6. Contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls if you have additional questions regarding this device safety notice.

Your Remedy Options

๐Ÿ“‹Other Action

Professional support and technical guidance

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: MEERA CL mobile operating table (Item 720001B0)
Model / REF:
720001B0
Lot Numbers:
S/N: 11399 through 11746
Product: MEERA CL mobile operating table (Item 720001B2)
Model / REF:
720001B2
Lot Numbers:
S/N: 10894 - 11128
Product: MEERA CL mobile operating table (Item 720001F0)
Model / REF:
720001F0
Lot Numbers:
S/N: 1059 through 1091
Product: MEERA CL mobile operating table (Item 720001F2)
Model / REF:
720001F2
Lot Numbers:
S/N: 579 - 639
Product: MEERA CL mobile operating table (Item 710001B0)
Model / REF:
710001B0
Lot Numbers:
S/N: 680 through 707
Product: MEERA CL mobile operating table (Item 710001B2)
Model / REF:
710001B2
Lot Numbers:
S/N: 252 - 254
Product: MEERA CL mobile operating table (Item 700001B0)
Model / REF:
700001B0
Lot Numbers:
S/N: 491 - 603
Product: MEERA CL mobile operating table (Item 700001F0)
Model / REF:
700001F0
Lot Numbers:
S/N: 9

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95498
Status: Active
Manufacturer: Getinge Usa Sales Inc
Sold By: Authorized Medical Device Distributors; Getinge Direct Sales
Manufactured In: United States
Units Affected: 8 products (342 units; 234 units; 22 units; 52 units; 112 units; 3 units; 112 units; 1 unit)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.