Lower riskMedical device recall · FDA · Published May 29, 2024
Getinge ALPHAMAXX Mobile Operating Table Charger Recall: Risk of Charging Failure
Getinge recalls ALPHAMAXX mobile operating tables with defective chargers that may cause charging failure. Affected models include 1133.22B4, 1133.22B5, and 1133.22F5 with specific serial numbers. No remedy is stated in the recall notice.
The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
Take action
Contact the company
📍Recalling firmGetinge Usa Sales Inc1 Geoffrey Way · Wayne, NJ 07470-2035
“Getinge ALPHAMAXX Mobile Operating Table Charger Recall: Risk of Charging Failure.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54980-getinge-alphamaxx-mobile-operating-table-charger-recall-risk-of-charging. Based on FDA recall #Z-2271-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2271-2024%22&limit=1).
The FDA announced on May 29, 2024, that Getinge Usa Sales Inc is recalling ALPHAMAXX Mobile Operating Tables due to a defective charger unit posing a risk of inadequate charging and operational failure. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Getinge
Product: ALPHAMAXX Mobile Operating Table
Model Number/Part Number: 113322B4
Serial Numbers: 3018 through 3078, 3080 through 3086, 3088 through 3089, 3095 through 3097
The hazard
The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
Context
GovInfoNow's records show Getinge Usa Sales Inc has had 16 other recalls on record since December 9, 2021. Other recent recalls include the Getinge Vaporizer Sevoflurane Recall (January 15, 2025), the Getinge MEERA CL Mobile Operating Table Recall (October 3, 2024), and another Getinge Vaporizer Sevoflurane Risk recall (May 1, 2024).
How to tell if you have this one
Check for model numbers 1133.22B4, 1133.22B5, or 1133.22F5 on the ALPHAMAXX mobile operating table. Serial numbers 3018 through 3078, 3080 through 3086, 3088 through 3089, or 3095 through 3097 indicate affected units.
Brand
Getinge
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech Republic, Denmark, France, Greece, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Mexico, New Zealand, Norway, Poland, Romania, Saudi Arabia, South Africa, Spain, Switzerland, Thailand, United Arab Emirates, United Kingdom.
Recall number
Product, codes & lots
Quantity
Z-2271-2024
ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4; Model Number/Part Number: 113322B4; UDI/DI: 04046768040007; Serial Numbers: 3018 through 3078, 3080 through 3086, 3088 through 3089, 3095 through 3097.
73 units
Z-2272-2024
ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B5; Model Number/Part Number: 113322B5; UDI/DI: 04046768040014; Serial Numbers: 2059 through 2183, 2185 through 2204, 2206, 2208, 2209, 2211 through 2231, 2233, 2235.
171 Units
Z-2273-2024
ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322F5; Model Number/Part Number: 113322F5; UDI/DI: 04046768040052; Serial Numbers: 409 through 411, 413 through 416.
7 units
Based on the official FDA remedy
What to do — step by step
Check Charger Model
Verify the charger model number is 0970.2873 to confirm if it's defective.
Where it went and when
Where it was distributed
Distributed in 4 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech Republic, Denmark, France, Greece, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Mexico, New Zealand, Norway, Poland, Romania, Saudi Arabia, South Africa,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Kentucky, New York, North Carolina, Virginia.
Recall timeline
FDA published this recall 49 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-2271-2024 (May 29, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2271-2024 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.