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.
Getinge is recalling ALPHAMAXX mobile operating tables with a defective charger that could cause charging failure. This means the tables might not work properly, which could affect medical procedures or equipment operation.
The defective charger unit (0970.2873) may not charge properly, leading to operational failure. This could cause medical equipment to stop working during critical procedures, potentially disrupting patient care.
Medical facilities using ALPHAMAXX mobile operating tables with specific model numbers and serial numbers are most at risk. Patients and staff could be affected if the tables fail during procedures.
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.
Verify the charger model number is 0970.2873 to confirm if it's defective.
The recall notice does not state any remedy for the defective charger.
Models 1133.22B4, 1133.22B5, and 1133.22F5 with specific serial numbers are affected.
Check the model number and serial numbers listed in the recall notice.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-2271-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-2271-2024 from Getinge. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
