Z-0153-2007

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

Name: Z-0153-2007 Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201...
Creator: Precision Medical, Inc.
Published: 2006-10-04
License: https://open.fda.gov/license/

Precision Medical, Inc. / initiated 2006-10-04 / Terminated

FDA source

Precision Medical, Inc. began a recall of Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201, Precision Medical, Inc., Northampton, PA 18067 on 2006-10-04. The reason FDA records is "Component assembly; The fill chuck is not assembled properly which may allow the device to come apart over time releasing its contents". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0153-2007
Status: Terminated
Initiated: 2006-10-04
Posted: 2006-11-04
Terminated: 2008-02-15
Recalling firm: Precision Medical, Inc.
Product: Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201, Precision Medical, Inc., Northampton, PA 18067
Product code: BYJ Unit, Liquid-Oxygen, Portable
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.
FDA root cause: Other
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.
Quantity in commerce: 550 units
Distribution: The product was shipped to home care providers nationwide
Product codes and lots: PM2200 Series. Model number 2201. Serial numbers P002892 through P005116

Product code BYJ

K041122Class IIPrecision Liquid Oxygen SystemPrecision Medical, Inc. / cleared 2004-10-04

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)