Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201, Precision Med
FDA device recall Z-0153-2007 · posted 2006-11-04 · Terminated
Recall details
- Recalling firm
- Precision Medical, Inc.
- 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.
- Action taken
- 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
- Status
- Terminated
- Product code
- BYJ
- Quantity affected
- 550 units
- Distribution
- The product was shipped to home care providers nationwide
- Date initiated
- 2006-10-04
- Date posted
- 2006-11-04
- Date terminated
- 2008-02-15
- Location
- Northampton, PA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| PRECISION LIQUID OXYGEN SYSTEM (K041122) | Precision Medical, Inc. | 2004-10-04 |