# FDA recall Z-2748-2026

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

## Product

MEDLINE convenience kits labeled as:    1) C-SECTION, Medline SKU DYNJ910835;   2) C-SECTION, Medline SKU DYNJ910835A; medical convenience kits

## Reason for recall

Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.

## Distribution

US:  OH, CA, IL, IN, FL, SC, AZ, NJ.

## Key facts

- **Recall number:** Z-2748-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-05
- **Report date:** 2026-07-29

- **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-2748-2026

## Citation

> AI Analytics. FDA recall Z-2748-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2748-2026. Source: US FDA. Licensed CC0.

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