# FDA recall Z-0451-2026

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

## Product

Convenience kits;  DYNJ901047R	ORTHO SPINE FUMICH  DYNJ902308K	TOTAL JOINT  DYNJ909111F	DR SALMA'S SPINE  DYNJ909117G	PATTERSON TOTAL JOINT  DYNJ909113F	KYPHOPLASTY

## 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-0451-2026
- **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-0451-2026

## Citation

> AI Analytics. FDA recall Z-0451-2026. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-0451-2026. Source: US FDA. Licensed CC0.

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