# FDA recall Z-0921-2026

> **Medline Industries, LP** · Class II · device recall initiated 2025-11-13.

## Product

SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000

## Reason for recall

The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.

## Distribution

US Nationwide distribution in the states CA, CO, IL, KS, and MI.

## Key facts

- **Recall number:** Z-0921-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-13
- **Report date:** 2025-12-24

- **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-0921-2026

## Citation

> AI Analytics. FDA recall Z-0921-2026. Retrieved 2026-09-21 from https://api.ai-analytics.org/recall/Z-0921-2026. Source: US FDA. Licensed CC0.

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