Atlas FDA

Circuit-Unilimb, Pediatric, 1M (40''), Disposable, Clean Non-Sterile, Pediatric Anesthesia Circuit, Part Number DYNJAPF4

FDA device recall Z-0761-05 · 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

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.