# FDA recall Z-2670-2025

> **Medline Industries, LP** · Class I · device recall initiated 2025-08-21.

## Product

Medline Kits:  1) VALVE PACK-LF, Model Number: DYNJ0415366P;   2) VALVE PACK-LF, Model Number: DYNJ0415366Q

## Reason for recall

The kits contain certain lots of cannula products where the catheter may not retain its shape.

## Distribution

US Nationwide distribution in the state of CA.

## Key facts

- **Recall number:** Z-2670-2025
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-21
- **Report date:** 2025-10-08

- **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-2670-2025

## Citation

> AI Analytics. FDA recall Z-2670-2025. Retrieved 2026-08-20 from https://api.ai-analytics.org/recall/Z-2670-2025. Source: US FDA. Licensed CC0.

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