FDA Recall
Terminated
Meridian Nexus- Pediatric, single use Part Numbers 60211-1304042, 60111-1, 60111-1MN, 40111-13042, 15900, 40010-1, and 40111-1. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
Recall: Z-0763-05
·
Initiated February 21, 2005
Recall
- Recall Number
- Z-0763-05
- Event Number
- 31451
- Firm
- MMS Sales Corp
- FEI Number
- 3004752896
- Product Code
- CAI
- Status
- Terminated
- Root Cause
- Other
- Initiated
- February 21, 2005
- Posted
- April 27, 2005
- Terminated
- December 20, 2006
- Address
- 218 Highline Rd, Pharr, TX, 78577-9726
Description
Meridian Nexus- Pediatric, single use Part Numbers 60211-1304042, 60111-1, 60111-1MN, 40111-13042, 15900, 40010-1, and 40111-1. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
Reason
Partial occlusion in the T-piece resulting in airway obstruction.
Action
The firm initiated the recall on February 21, 2004 by letter to all consignees.
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
Quantity
Total for all products: 7455 cases (161,273 units)