Custom Kit
FDA device recall Z-0913-03 · posted 2003-06-05 · Terminated
Recall details
- Recalling firm
- Merit Medical Systems, Inc
- Reason for recall
- Cracks in the syringe barrels could allow for air aspiration into the syringe barrel.
- Action taken
- On 5/16/2003, all distributors and consignees were notified by letter.
- Root cause
- Other
- Status
- Terminated
- Product code
- DQO
- Quantity affected
- 20 kits
- Distribution
- Nationwide. Foreign distribution to France, Malaysia, Taiwan, Dominican Republic.
- Date initiated
- 2003-05-16
- Date posted
- 2003-06-05
- Date terminated
- 2003-07-21
- Location
- South Jordan, UT
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.