MMS Sales Corp 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
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
MMS Sales Corp
Lot Codes / Batch Numbers
Part Number 15900, 20 per case, Lot Numbers: 571671004, Part Number 40010-1, 20 per case, Lot Numbers: 568901004, 581081104, Part Number 40111-1, 20 per case, Lot Numbers: 575701104, Part Number 40111-13042, 20 per case, Lot Numbers: 564430904, 580031104, Part Number 60111-1, 20 per case, Lot Numbers: 594870105, Part Number 60111-1MN, 20 per case, Lot Numbers: 569701004, Part Number 60211-1304042, 15 per case, Lot Numbers: 591400105
Products Sold
Part Number 15900, 20 per case, Lot Numbers: 571671004; Part Number 40010-1, 20 per case, Lot Numbers: 568901004, 581081104; Part Number 40111-1, 20 per case, Lot Numbers: 575701104; Part Number 40111-13042, 20 per case, Lot Numbers: 564430904, 580031104; Part Number 60111-1, 20 per case, Lot Numbers: 594870105; Part Number 60111-1MN, 20 per case, Lot Numbers: 569701004; Part Number 60211-1304042, 15 per case, Lot Numbers: 591400105
MMS Sales Corp is recalling Meridian Nexus- Pediatric, single use Part Numbers 60211-1304042, 60111-1, 60111-1MN, 40111-13042, 1 due to Partial occlusion in the T-piece resulting in airway obstruction.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Partial occlusion in the T-piece resulting in airway obstruction.
Recommended Action
Per FDA guidance
The firm initiated the recall on February 21, 2004 by letter to all consignees.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, CO, FL, IL, IN, MI, OH, OR, UT, VA
Page updated: Jan 10, 2026