Kendall MONOJECT MAGELLAN SAFETY NEEDLE 18G X 1 inch Produt Number: 8881850815
FDA device recall Z-0083-05 · 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
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