FDA Medical Device Recalls (openFDA)
MMS Sales Corp: Circuit-Nexus, Adult, single use, Part Numbers: N7A110CG06, N4A100CE06, C4N0121000, 60010-1B, and 40301-1-2730. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
- Recall number
- Z-0766-05
- Recalling firm
- MMS Sales Corp
- Product
- Circuit-Nexus, Adult, single use, Part Numbers: N7A110CG06, N4A100CE06, C4N0121000, 60010-1B, and 40301-1-2730. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
- Status
- Terminated
- Initiated
- 2005-02-21
- Posted
- 2005-04-27
- Terminated
- 2006-12-20
- Reason
- Partial occlusion in the T-piece resulting in airway obstruction.
- Root cause
- Other
- Action
- The firm initiated the recall on February 21, 2004 by letter to all consignees.
- Quantity
- 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
- Lot, serial or model codes
- Part Number C4N0121000, 40 per case, Lot Number: 587021204, 587031204, 588371204, 591070105, 596840105; Part Number N4A100CE06, 20 per case, Lot Number: 575741104; Part Number N7A110CG06, 15 per case, Lot Number: 596700105; Part Number 40301-1-2730, 20 per case, Lot Number: 564460904, 566310904, 568481004, 570271004, 571911004, 573261004, 577091104, 580061104, 582711204, 588561204, 589270105, 596290105; Part Number 60010-1B, 60 per case, Lot Number: 575691104, 579871104, 585041204, 586291204
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- CAI
- Firm FEI
- 3004752896
- Firm city
- Pharr
- Firm state
- TX
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28