# FDA recall Z-2454-2026

> **Medline Industries, LP** · Class I · device recall initiated 2026-05-06.

## Product

Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142;   2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407

## Reason for recall

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

## Distribution

US Nationwide.

## Key facts

- **Recall number:** Z-2454-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-06
- **Report date:** 2026-07-01

- **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-2454-2026

## Citation

> MORVS. FDA recall Z-2454-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2454-2026. Source: US FDA. Licensed CC0.

---

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