Reported Sep 23, 2026 · Ongoing

Medline Convenience Kits

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?

Medline Convenience Kits

17 of 17 products

Products covered by this recall
Model / numberProduct as published
DYNDB3086DDYNDB3086D
DYNDB3100DYNDB3100
DYNDH1619ADYNDH1619A
DYNDH1620ADYNDH1620A
DYNDH1694ADYNDH1694A
DYNDH1695DYNDH1695
DYNDH1708ADYNDH1708A
DYNDH1714ADYNDH1714A
DYNDH1723DYNDH1723
DYNDH1740BDYNDH1740B
DYNDH1741BDYNDH1741B
DYNDH1771ADYNDH1771A
DYNDH1908DYNDH1908
DYNDH1940DYNDH1940
DYNDH1988DYNDH1988
DYNDH2002DYNDH2002
DYNDH2017.DYNDH2017, Blood and urine collection kits
Lot codes and dates

29 of 29 products

Products covered by this recall
#BarcodesProduct as published
11019845902891540198459028916Lot Number: 24IBA685; 2) DYNDB3100, UDI-DI: 10198459028915(each), 40198459028916(case)
21019532721583540195327215836Lot Number: 24IBF913; 3) DYNDH1619A, UDI-DI: 10195327215835(each), 40195327215836(case)
31019532721583540195327215836Lot Number: 24FBH708; 4) DYNDH1619A, UDI-DI: 10195327215835(each), 40195327215836(case)
41019532721604740195327216048Lot Number: 24HBG622; 5) DYNDH1620A, UDI-DI: 10195327216047(each), 40195327216048(case)
51019532721604740195327216048Lot Number: 24GBY827; 6) DYNDH1620A, UDI-DI: 10195327216047(each), 40195327216048(case)
61019532721604740195327216048Lot Number: 24HBQ593; 7) DYNDH1620A, UDI-DI: 10195327216047(each), 40195327216048(case)
71019532713995740195327139958Lot Number: 24HBU881; 8) DYNDH1694A, UDI-DI: 10195327139957(each), 40195327139958(case)
81019532713995740195327139958Lot Number: 24EBI901; 9) DYNDH1694A, UDI-DI: 10195327139957(each), 40195327139958(case)
91019532711315540195327113156Lot Number: 24HBG834; 10) DYNDH1695, UDI-DI: 10195327113155(each), 40195327113156(case)
101019532749836840195327498369Lot Number: 24FBQ907; 11) DYNDH1708A, UDI-DI: 10195327498368(each), 40195327498369(case)
111019532734755040195327347551Lot Number: 24IBQ580; 12) DYNDH1714A, UDI-DI: 10195327347550(each), 40195327347551(case)
121019532734755040195327347551Lot Number: 24EBI892; 13) DYNDH1714A, UDI-DI: 10195327347550(each), 40195327347551(case)
131019532713420440195327134205Lot Number: 24IBE380; 14) DYNDH1723, UDI-DI: 10195327134204(each), 40195327134205(case)
141019532713420440195327134205Lot Number: 24EBI893; 15) DYNDH1723, UDI-DI: 10195327134204(each), 40195327134205(case)
151019532713420440195327134205Lot Number: 24GBH135; 16) DYNDH1723, UDI-DI: 10195327134204(each), 40195327134205(case)
161019845900630240198459006303Lot Number: 24HBG826; 17) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case)
171019845900630240198459006303Lot Number: 24EBV834; 18) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case)
181019845900630240198459006303Lot Number: 24FBH710; 19) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case)
191019845900630240198459006303Lot Number: 24FBK197; 20) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case)
201019845900631940198459006310Lot Number: 24GBW340; 21) DYNDH1741B, UDI-DI: 10198459006319(each), 40198459006310(case)
Amount recalled
47848 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

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.

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

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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 (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Notice updated Sep 15, 2026 · Data as of Sep 19, 2:56 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.