# FDA recall Z-2537-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-05-21.

## Product

Medline Convenience Kits:  1) DYNJ0621189X, Model Number: SM RADIOLOGY-ANGIO PACK-LF;   2) PAIN1470A, Model Number: CONT. 20G EPI MRI COMPATIBLE;   3) TVS4000L, Model Number: TVS4000 ENDOVENOUS PACK

## Reason for recall

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2537-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-21
- **Report date:** 2026-07-08

- **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-2537-2026

## Citation

> MORVS. FDA recall Z-2537-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2537-2026. Source: US FDA. Licensed CC0.

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