Reported Apr 29, 2026 · Ongoing

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A,…

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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?

3 of 3 products

Products covered by this recall
Model / numberProduct as published
DYNJ38587AMedline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK
DYNJ30078DTRAY-LF
DYNJ59108BW LINQ PACK
Lot codes and dates
  • DYNJ38587A UDI-DI 10193489754070 (EA) 40193489754071 (CS) LOTS
    • 20BBF696
    • 20EBH917
    • 20FBW435
    • 20HBM667
    • 20JBF107
    • 20KBW292
    • 20LBS930
    • 21EBB195
    • 21FBR610
    • 21GBS936
    • 21GBS940
    • 21JBU912
    • 21KBP999
    • 22ABX182
    • 22EBI922
    • 22GBZ788
    • 22JBL031
    • 23BBN160
    • DYNJ38587B
    UDI-DI 10195327397326 (EA) 40195327397327 (CS) LOTS
    • 23DBP789
    • 23FBM124
    • 23HBW639
    • 23JBN841
    • 24ABG236
    • 24CBM867
    • 24FME120
    • 24JMD066
    • 24LME187
    • DYNJ30078D
    UDI-DI 10889942138647 (EA) 40889942138648 (CS) LOTS
    • 23CBK546
    • 23FBQ481
    • 23IBQ435
    • 23JBR634
    • 23LBG856
    • 24ABE287
    • 24BBS264
    • 24EBQ336
    • 24GBJ987
    • 24JBO830
    • DYNJ59108B
    UDI-DI 10198459138461 (EA) 40198459138462 (CS) LOT 24JBP861 ***Updated 5/20/26 - The following lots were included in the customer communication but not in the FDA submission.*** DYNJ30078D Lots
    • 21EBD861
    • 21IBM130
    • 21IBV938
    • 21IBV939
    • 21IBV940
    • 21LBB809
    • 22ABZ810
    • 22BBV614
    • 22FBL865
    • 22IBE477
    • 22JBH508
    • 22KBJ437
    • 22OBC310
    • 23BBT881
    23EBK298; DYNJ38587B Lots 25BMB873; DYNJ59108B Lots 24LBT539
Amount recalled
270,311 total

This recall covers 39 products

The agency filed one notice per product. You are reading one of them; the other 38 are below.

26 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Unapproved design changes to the products outside of the 510(k) clearance.

This product could cause temporary or reversible health problems — stop using it.

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, 6:55 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.