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Terminated

Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201, Precision Medical, Inc., Northampton, PA 18067

FDA Recall Z-0153-2007 · Posted 2006-11-04

Recall StatusTerminated
Product CodeBYJ
Date Initiated2006-10-04
Date Terminated2008-02-15
Product Quantity550 units

Reason for Recall

Component assembly; The fill chuck is not assembled properly which may allow the device to come apart over time releasing its contents.

Firm Action

The recalling firm telephoned the company to inform them of the problem and to make them aware that replacements would be made available starting on 10/16/06.

Root Cause

Other

Distribution Pattern

The product was shipped to home care providers nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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