# FDA recall Z-0442-2026

> **Medline Industries, LP** · Class I · device recall initiated 2025-10-10.

## 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.

## Distribution

International distribution to Mexico and Panama. US nationwide distribution to the following: AK AL AR AZ CA CO CT FL GA IA IL IN KS KY MA ME MI MN MO MS MT NC NJ NY OH OR PA PR RI SC TN TX WA WI;

## Key facts

- **Recall number:** Z-0442-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-10
- **Report date:** 2025-11-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0442-2026

## Citation

> AI Analytics. FDA recall Z-0442-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0442-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*