Data Foundry

Medical device recalls 2026

MEDLINE convenience kits labeled as: 1) C-SECTION — Class I medical device recall Z-2748-2026

Ongoing recall by Medline Industries, LP, reported 2026-07-29, distributed in AZ, CA, FL, IL, IN, NJ, OH, SC. Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that

Recall numberZ-2748-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-06-05
Classified2026-07-22
Reported by FDA2026-07-29
DistributedAZ, CA, FL, IL, IN, NJ, OH, SC
Quantity56 kits
UPC / GTIN / UDI-DI10198459152849, 10198459252570, 40198459152840, 40198459252571
Lot numbers25BBC541, 25DBP805

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2748-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.