[Recalled] CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit — An audit discovered some inconsistencies in weld penetration on the longitudina… | FDA 2022-10-10

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: 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.

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from Caire, Inc.

• CAIRE FreeStyle Comfort Portable Oxygen Concentrator with autoSAT, UltraSense and autoDOSE, model #AS200-3 — Class II
• CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2. — Class II
• CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit — Class I
• CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The FreeStyle Comfort Oxygen Concentrator is intended for the administration of supplemental oxygen. The device is not intended for life support nor does it provide any patient monitoring capabilities. — Class II
• CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit — Class I

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.