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?

81 of 81 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 26AMH714
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 26AMF179
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 25IMI476
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 25GME934
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 24JMA156
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 24IMG162
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 23IBG784
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 23HBG512
DYNJRA02451088438957348840884389573489Medline : UDI/DI 10884389573488 each, 40884389573489 case, Lot Number 23HBA325
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 26AMK307
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25LME383
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25JMJ632
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25IMI508
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25IMB093
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25GMB270
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25EMD040
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 25EMB958
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24HMD548
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24HMA551
DYNJRA05551088827727092340888277270924Medline : UDI/DI 10888277270923 each, 40888277270924 case, Lot Number 24GMI471
Amount recalled
41720 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, 5:36 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.