Kendall MONOJECT MAGELLAN 12cc Syringe with Safety Needle 22G X 1.5 inch Product Number: 5551822215
FDA device recall Z-0111-05 · posted 2004-11-02 · Terminated
Recall details
- Recalling firm
- Kendall Healthcare Products Co
- Reason for recall
- Needle cannula may separate from the hub during use
- Action taken
- Recall letters requesting product return were mailed to all customers on October 8, 2004
- Root cause
- Other
- Status
- Terminated
- Product code
- FMI
- Distribution
- Nationwide
- Date initiated
- 2004-10-08
- Date posted
- 2004-11-02
- Date terminated
- 2012-05-15
- Location
- Mansfield, MA
Monitor recalls programmatically
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MONOJECT SAFETY NEEDLE (K012736) | Tyco Healthcare | 2001-10-25 |