Reported Jul 29, 2026 · Ongoing

MEDLINE convenience kits labeled as

Medline Industries, LP

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

63 of 63 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYKS1574A1019845914744940198459147440Medline Kit , UDI/DI 10198459147449 (each) 40198459147440 (case), Kit Lot Number 25ELB079
DYKS1574A1019845914744940198459147440Medline Kit , UDI/DI 10198459147449 (each) 40198459147440 (case), Kit Lot Number 25DLA930
DYNJ902378J1019845912881340198459128814Medline Kit , UDI/DI 10198459128813 (each) 40198459128814 (case), Kit Lot Number 25IBN992
DYNJ902378J1019845912881340198459128814Medline Kit , UDI/DI 10198459128813 (each) 40198459128814 (case), Kit Lot Number 25HBS205
DYNJ902378J1019845912881340198459128814Medline Kit , UDI/DI 10198459128813 (each) 40198459128814 (case), Kit Lot Number 25DBH984
DYNJ902378J1019845912881340198459128814Medline Kit , UDI/DI 10198459128813 (each) 40198459128814 (case), Kit Lot Number 25CBB436
DYNJ902378J1019845912881340198459128814Medline Kit , UDI/DI 10198459128813 (each) 40198459128814 (case), Kit Lot Number 25ABR220
DYNJ902378J1019845912881340198459128814Medline Kit , UDI/DI 10198459128813 (each) 40198459128814 (case), Kit Lot Number 24LBI991
DYNJ903492K1019845925519940198459255190Medline Kit , UDI/DI 10198459255199 (each) 40198459255190 (case), Kit Lot Number 25CBR847
DYNJ903492K1019845925519940198459255190Medline Kit , UDI/DI 10198459255199 (each) 40198459255190 (case), Kit Lot Number 25CBE741
DYNJ903493I1019532756551040195327565511Medline Kit , UDI/DI 10195327565510 (each) 40195327565511 (case), Kit Lot Number 25ADA380
DYNJ903493I1019532756551040195327565511Medline Kit , UDI/DI 10195327565510 (each) 40195327565511 (case), Kit Lot Number 24KDA993
DYNJ903493J1019845925505240198459255053Medline Kit , UDI/DI 10198459255052 (each) 40198459255053 (case), Kit Lot Number 25CDA748
DYNJ903493J1019845925505240198459255053Medline Kit , UDI/DI 10198459255052 (each) 40198459255053 (case), Kit Lot Number 25CDA157
DYNJ903493K1019845929312240198459293123Medline Kit , UDI/DI 10198459293122 (each) 40198459293123 (case), Kit Lot Number 25DDA444
DYNJ906665G1019532709248140195327092482Medline Kit , UDI/DI 10195327092481 (each) 40195327092482 (case), Kit Lot Number 25GDA109
DYNJ906665G1019532709248140195327092482Medline Kit , UDI/DI 10195327092481 (each) 40195327092482 (case), Kit Lot Number 25FDB471
DYNJ906665G1019532709248140195327092482Medline Kit , UDI/DI 10195327092481 (each) 40195327092482 (case), Kit Lot Number 25EDB817
DYNJ906665G1019532709248140195327092482Medline Kit , UDI/DI 10195327092481 (each) 40195327092482 (case), Kit Lot Number 25BDA465
DYNJ906665G1019532709248140195327092482Medline Kit , UDI/DI 10195327092481 (each) 40195327092482 (case), Kit Lot Number 24LDB209
Amount recalled
2301 kits

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

Why it was recalled

Stop using this product now

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.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:42 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.