Reported Nov 19, 2025 · Ongoing
Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers:…
Medline Industries, LP
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
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Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers
14 of 14 products
| # | Product as published |
|---|---|
| 1 | ADULT 120 EXPANDABLE W/MASK DYNJAA10591 |
| 2 | ANES CIRC 120IN EXP-LF DYNJAA6555G |
| 3 | ANES CIRCUIT ADULT 120"-LF DYNJAA10817 |
| 4 | ANESTHESIA 120" ADLT-LF DYNJAA10775 |
| 5 | ANESTHESIA CIRC ADULT 120-LF DYNJAA10601 |
| 6 | ANESTHESIA CIRCUIT - LF DYNJAA10261B |
| 7 | ANESTHESIA CIRCUIT 120EXP-LF DYNJAA10741A |
| 8 | ANESTHESIA CIRCUIT ADULT-LF DYNJAA0380A DYNJAA10641 DYNJAA10706B DYNJAA10851 DYNJAA10922B DYNJAA10971A DYNJAA11030A DYNJAA11087 DYNJAA11126 |
| 9 | ANESTHESIA CIRCUIT-LF DYNJAA0309A DYNJAA0368A DYNJAA10368A DYNJAA10392 DYNJAA10430A DYNJAA10547A DYNJAA10639A DYNJAA10656A DYNJAA10685A DYNJAA10685B |
| 10 | CIRC 120" EXP 1 BV HMEF 3L GSL DYNJAA10920 |
| 11 | EXPANDABLE CIRCUIT-LF DYNJAA11095 |
| 12 | NM ANESTHESIA TURNOVER KIT DYNJAA0433 |
| 13 | PROV HEALTH HEPA CIRC #2-LF DYNJAA0360 |
| 14 | SPTMPX01IA CIRCUIT ADULT-LF DYNJAA10973A |
- Lot codes and dates
31 of 31 products
Products covered by this recall # Barcodes Product as published 1 4019348940026810193489400267DYNJAA0309A UDI-DI 40193489400268 (case), 10193489400267 (ea) Lots 25EBU353 25GBI473 2 4019348941900010193489419009DYNJAA0360 UDI DI 40193489419000 (case), 10193489419009 (ea) Lots 25EBU304 25GBQ732 3 4019532709255010195327092559DYNJAA0368A UDI-DI 40195327092550 (case), 10195327092559 (ea) Lots 25GBH582 4 4019532747828610195327478285DYNJAA0380A UDI-DI 40195327478286 (case), 10195327478285 (ea) Lots 25FBB950 25FBT875 25GBX623 5 4019845932070610198459320705DYNJAA0433 UDI-DI 40198459320706 (case), 10198459320705 (ea) Lots 25EBH621 25EBQ391 6 4019348943078410193489430783DYNJAA10261B UDI- DI 40193489430784 (case), 10193489430783 (ea) Lots 25FBJ760 7 4019845932072010198459320729DYNJAA10368A UDI-DI 40198459320720 (case), 10198459320729 (ea) Lots 25GBY374 25IBK072 8 4088827796220110888277962200DYNJAA10392 UDI-DI 40888277962201 (case), 10888277962200 (ea) Lots 25FBN032 9 4019348983205210193489832051DYNJAA10430A UDI-DI 40193489832052 (case), 10193489832051 (ea) Lots 25FBW335 25IBH048 10 4019348960318810193489603187DYNJAA10547A UDI-DI 40193489603188 (case), 10193489603187 (ea) 25FBT853 11 4088994263253510889942632534DYNJAA10591 UDI-DI 40889942632535 (case), 10889942632534 (ea) Lots 25FBD876 25FBD877 25GBJ254 25GBJ256 12 4088994265543510889942655434DYNJAA10601 UDI-DI 40889942655435 (case), 10889942655434 (ea) Lots 25FBN184 25HBM893 13 4088827776195810888277761957DYNJAA10639A UDI-DI 40888277761958 (case), 10888277761957 (ea) Lots 25FBN043 14 4088994284122710889942841226DYNJAA10641 UDI-DI 40889942841227 (case), 10889942841226 (ea) Lots 25EBK360 15 4019348945552710193489455526DYNJAA10656A UDI-DI 40193489455527 (case), 10193489455526 (ea) Lots 25FBN055 16 4019532727914210195327279141DYNJAA10685A UDI-DI 40195327279142 (case), 10195327279141 (ea) Lots 25EBJ456 17 4019845937229310198459372292DYNJAA10685B UDI-DI 40198459372293 (case), 10198459372292 (ea) Lots 25FBL121 25FBT898 25FBT899 18 4019348948598210193489485981DYNJAA10706B UDI-DI 40193489485982 (case), 10193489485981 (ea) Lots 25FBH921 25GBK879 25GBN124 25GBN125 19 4019348925057310193489250572DYNJAA10741A UDI-DI 40193489250573 (case), 10193489250572 (ea) Lots 25EBK364 25FBQ326 25HBA472 20 4019348934810210193489348101DYNJAA10775 UDI-DI 40193489348102 (case), 10193489348101 (ea) Lots 25GBY311 25IBD803 - Amount recalled
- 96,406 total units
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
Why it was recalled
Stop using this product now
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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