Meridian Nexus- Pediatric, single use Part Numbers 60211-1304042, 60111-1, 60111-1MN, 40111-13042, 15900, 40010-1, and 4
FDA device recall Z-0763-05 · posted 2005-04-27 · Terminated
Recall details
- Recalling firm
- MMS Sales Corp
- Reason for recall
- Partial occlusion in the T-piece resulting in airway obstruction.
- Action taken
- The firm initiated the recall on February 21, 2004 by letter to all consignees.
- Root cause
- Other
- Status
- Terminated
- Product code
- CAI
- Quantity affected
- Total for all products: 7455 cases (161,273 units)
- Distribution
- Product was distributed domestically to customers in CA, AZ, IL, CO, OR, FL, VA, OH, MI, and UT. Product was also distributed to the following foreign countries: Malaysia, Mexico, and New Zealand
- Date initiated
- 2005-02-21
- Date posted
- 2005-04-27
- Date terminated
- 2006-12-20
- Location
- Pharr, TX
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