FDA Medical Device Recalls (openFDA)
Precision Medical, Inc.: Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201, Precision Medical, Inc., Northampton, PA 18067
- Recall number
- Z-0153-2007
- 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
- Status
- Terminated
- Initiated
- 2006-10-04
- Posted
- 2006-11-04
- Terminated
- 2008-02-15
- Reason
- Component assembly; The fill chuck is not assembled properly which may allow the device to come apart over time releasing its contents.
- 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
- 550 units
- Distribution
- The product was shipped to home care providers nationwide
- Lot, serial or model codes
- PM2200 Series. Model number 2201. Serial numbers P002892 through P005116
- 510(k) numbers
- ["K041122"]
- PMA numbers
- not on file
- Product code
- BYJ
- Firm FEI
- 2523148
- Firm city
- Northampton
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28