Medline Industries, Inc. Medline Custom Anesthesia Set Up Kit - Latex Free (non-sterile), reorder number DYNJAA0078C; the kit contains the Nexus Adult Unilimb Circuit - 40'', part C4N000D001, along with a 3 liter latex free breathing bag, suction catheter, adult medium anesthesia mask, suction tubing, humid vent hme filter and poly bag; Made in USA by Medline Industries, Inc., Mundelein, IL 60060 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline Custom Anesthesia Set Up Kit - Latex Free (non-sterile), reorder number DYNJAA0078C; the kit contains the Nexus Adult Unilimb Circuit - 40'', part C4N000D001, along with a 3 liter latex free breathing bag, suction catheter, adult medium anesthesia mask, suction tubing, humid vent hme filter and poly bag; Made in USA by Medline Industries, Inc., Mundelein, IL 60060
Brand
Medline Industries, Inc.
Lot Codes / Batch Numbers
reorder number DYNJAA0078C, lots 04KD3355, 04KD4186, 04KD4500, 04LD1866, 04LD2479, 04LD3673, 05AD3501, 05BD0357, 05BD4129
Products Sold
reorder number DYNJAA0078C, lots 04KD3355, 04KD4186, 04KD4500, 04LD1866, 04LD2479, 04LD3673, 05AD3501, 05BD0357, 05BD4129
Medline Industries, Inc. is recalling Medline Custom Anesthesia Set Up Kit - Latex Free (non-sterile), reorder number DYNJAA0078C; the kit due to The procedure packs contain anesthesia/breathing circuits being recalled by MMS Sales due to partial occlusion of the T-piece resulting in airway obst. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The procedure packs contain anesthesia/breathing circuits being recalled by MMS Sales due to partial occlusion of the T-piece resulting in airway obstruction.
Recommended Action
Per FDA guidance
Recalled from the direct account hospitals via letter dated 3/18/05 and 3/23/05. The letters informed the accounts of the occlusion via copy of the MMS recall letter, and listed the Medline reorder number and lot numbers of the custom packs shipped to them, along with the MMS part number contained there in. The accounts were requested to examine their stocks for the affected codes and return them to Medline.
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
AL, CA, FL, IN, MN
Page updated: Jan 10, 2026