Reported Jun 3, 2026 · Ongoing

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, 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?

71 of 71 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 26BBJ392
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 26ABS354
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25LBC413
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25IBK142
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25FBD584
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 25BBK828
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 24FBT398
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 24BBR608
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 23JBB581
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 23IBQ010
DYNJRA10971088994287923640889942879237Medline Kit : UDI/DI 10889942879236 each, 40889942879237 case, Lot Number 23HBM569
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 26AMK346
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25KMG102
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25JMA641
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25GMC349
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25DMG474
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25DMC357
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 25ADB659
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 24LDB606
DYNJRA11541088994293586440889942935865Medline Kit : UDI/DI 10889942935864 each, 40889942935865 case, Lot Number 24KDB682
Amount recalled
30120 kits

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 7:35 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.