CAIRE Liberator 30 recall
CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
Why was CAIRE Liberator 30 recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI M766133374030, Serial Numbers: CBB3022300368, CBB3022300390, CBB3022300470, CBB3022300472, CBB3022300479
- Product
- CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
- Recalling firm
- Caire, Inc.
- Quantity
- 5 devices
- Distribution
- US Nationwide - Worldwide Distribution: CA, NC, OH, AZ, and Canada, Chile, Colombia, and Germany
- Recall date
- December 14, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)