Anesthesia Circuit Kits and other various kits that contain… — Class I medical device recall Z-0442-2026
Ongoing recall by Medline Industries, LP, reported 2025-11-19, distributed nationwide. Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cra
| Recall number | Z-0442-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-10-10 |
| Classified | 2025-11-13 |
| Reported by FDA | 2025-11-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | MX, PA |
| Quantity | 96,406 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10193489250572, 10193489348101, 10193489365337, 10193489400267, 10193489419009, 10193489429466, 10193489430783, 10193489455526, 10193489463385, 10193489485981, 10193489603187, 10193489832051, 10195327092559, 10195327214647, 10195327279141, 10195327298166, 10195327341039, 10195327372422, 10195327478285, 10195327520991, 10195327694401, 10195327695507, 10198459301889, 10198459320705, 10198459320729 and 37 more |
| Lot numbers | 25EBG518, 25EBH621, 25EBJ456, 25EBK360, 25EBK364, 25EBQ391, 25EBU304, 25EBU353, 25EBV629, 25FBB950, 25FBD876, 25FBD877, 25FBG942, 25FBG944, 25FBH921, 25FBJ760, 25FBL121, 25FBN032, 25FBN043, 25FBN055, 25FBN184, 25FBQ326, 25FBQ346, 25FBQ349, 25FBQ442, 25FBS747, 25FBS748, 25FBT844, 25FBT875, 25FBT898, 25FBT899, 25FBW335, 25GBA751, 25GBE789, 25GBH582, 25GBI473, 25GBJ254, 25GBJ256, 25GBK879, 25GBL211 and 46 more |
Product
Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers: ADULT 120 EXPANDABLE W/MASK DYNJAA10591; ANES CIRC 120IN EXP-LF DYNJAA6555G; ANES CIRCUIT ADULT 120"-LF DYNJAA10817; ANESTHESIA 120" ADLT-LF DYNJAA10775; ANESTHESIA CIRC ADULT 120-LF DYNJAA10601; ANESTHESIA CIRCUIT - LF DYNJAA10261B; ANESTHESIA CIRCUIT 120EXP-LF DYNJAA10741A; ANESTHESIA CIRCUIT ADULT-LF DYNJAA0380A DYNJAA10641 DYNJAA10706B DYNJAA10851 DYNJAA10922B DYNJAA10971A DYNJAA11030A DYNJAA11087 DYNJAA11126; ANESTHESIA CIRCUIT-LF DYNJAA0309A DYNJAA0368A DYNJAA10368A DYNJAA10392 DYNJAA10430A DYNJAA10547A DYNJAA10639A DYNJAA10656A DYNJAA10685A DYNJAA10685B; CIRC 120" EXP 1 BV HMEF 3L GSL DYNJAA10920; EXPANDABLE CIRCUIT-LF DYNJAA11095; NM ANESTHESIA TURNOVER KIT DYNJAA0433; PROV HEALTH HEPA CIRC #2-LF DYNJAA0360; SPTMPX01IA CIRCUIT ADULT-LF DYNJAA10973A;
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0442-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.