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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: ALPHAMAXX Mobile Operating Tables Recalled Due to Charger Defect

Agency Publication Date: July 5, 2024
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Summary

Getinge USA Sales Inc. is recalling 251 ALPHAMAXX mobile operating tables due to a defective charging unit (part number 0970.2873). The issue affects models 113322B4, 113322B5, and 113322F5. This defect can lead to inadequate charging, causing the operating table to fail or stop functioning during use. Consumers should immediately check their device serial numbers and contact the manufacturer or their healthcare provider for instructions on how to handle affected units.

Risk

A defective charger can prevent the operating table's battery from charging properly, leading to operational failure. If the table loses power or fails to move during a medical procedure, it could result in surgical delays or compromised patient positioning.

What You Should Do

  1. Check your operating table's model number and serial number to see if it is affected by this recall. Affected model 113322B4 includes serial numbers 3018-3078, 3080-3086, 3088-3089, and 3095-3097.
  2. Check model 113322B5 for serial numbers 2059-2183, 2185-2204, 2206, 2208, 2209, 2211-2231, 2233, and 2235.
  3. Check model 113322F5 for serial numbers 409-411 and 413-416.
  4. Verify if the table is equipped with the defective charger unit (part number 0970.2873).
  5. Contact Getinge USA Sales Inc. at 1 Geoffrey Way, Wayne, New Jersey, 07470-2035, or contact your facility's biomedical engineering department to arrange for an inspection and correction of the defective charger.
  6. If you are a patient or healthcare provider with questions about the safety of this equipment, contact your medical facility or Getinge directly for further instructions.
  7. Contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional assistance or to report any device-related issues.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer initiated correction via notification letter.

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

Affected Products

Product: ALPHAMAXX Mobile Operating Table Model 113322B4
Model / REF:
113322B4
Lot Numbers:
Serial Numbers: 3018 through 3078, 3080 through 3086, 3088 through 3089, 3095 through 3097
UDI/DI: 04046768040007
Product: ALPHAMAXX Mobile Operating Table Model 113322B5
Model / REF:
113322B5
Lot Numbers:
Serial Numbers: 2059 through 2183, 2185 through 2204, 2206, 2208, 2209, 2211 through 2231, 2233, 2235
UDI/DI: 04046768040014
Product: ALPHAMAXX Mobile Operating Table Model 113322F5
Model / REF:
113322F5
Lot Numbers:
Serial Numbers: 409 through 411, 413 through 416
UDI/DI: 04046768040052

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94740
Status: Active
Manufacturer: Getinge Usa Sales Inc
Sold By: Authorized Medical Distributors; Getinge USA Sales Inc.
Manufactured In: United States
Units Affected: 3 products (73 units; 171 Units; 7 units)
Distributed To: Kentucky, North Carolina, New York, Virginia

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.