Caire recalls Liberator 20 liquid oxygen units with model 13256195 due to potential weld defects that could cause device failure. Affected units have specific serial numbers and UDI codes.
An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.
Caire is recalling some Liberator 20 liquid oxygen systems because welds on the inner bottle may be inconsistent. This could lead to device failure, but the recall does not specify immediate danger to users.
Inconsistent welds on the inner bottle could lead to leaks or device failure. However, the recall does not indicate that this causes immediate injury or serious harm during normal use.
Users of the Liberator 20 liquid oxygen system with model 13256195 and specific serial numbers are affected. Medical oxygen users are most at risk due to the device's critical function.
Check for the model number 13256195 and serial numbers CBB3022320073, CBB3022320077, or CBB3022320074. The UDI code M766133374030M766132561950 also identifies affected units.
Verify the model number and serial numbers listed in the recall to confirm if your unit is affected.
The recall mentions potential weld inconsistencies that could cause device failure, but it does not state that this leads to injury or serious harm during normal use.
Check for the model number 13256195 and serial numbers CBB3022320073, CBB3022320077, or CBB3022320074. The UDI code M766133374030M766132561950 also identifies affected units.
The recall does not specify a remedy, so affected users should check with Caire for further instructions.
We’ve drafted a message you can send Caire to request your refund or repair — edit it as you like.
Subject: Recall Z-0339-2023 — Caire Caire Hello, I own a Caire that is covered by recall Z-0339-2023 from Caire. 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.
