Reported Apr 29, 2026 · Ongoing

Medline Kits

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?

Medline Kits

41 of 41 products

Products covered by this recall
Model / numberProduct as published
DYKB1038NEWBORN ADMISSION
DYNDA3188DRAINAGE TRAY
DYNJG001027BVA ORLANDO SHOULDER PACK
TUMESCENT SYRINGE KIT, Model Number: DYNJTUMSYR
DYNJT3719OMC PTCA PACK
DYNJT5667PORT PACK
DYNJWASTEKIT2WASTE MANAGEMENT KIT - 2
DYNJ20175JCARDIAC CATH
DYNJ33521DD&C PACK-POB
DYNJ38533FBASIC PACK
DYNJ39230DCATH PACK IMPLANT
DYNJ40886BCERVICAL SPINE PACK
DYNJ41553FMV-IR ANGIO DRAPE PACK-LF
DYNJ41558DTV ENDOVASCULAR-LF
DYNJ44816JMAJOR PACK-LF
DYNJ48683AANGIOGRAPHY PACK
DYNJ55922CEXTREMITY PACK
DYNJ57785CNEURO PACK
DYNJ61377BPACEMAKER PACK
DYNJ62683DVASCULAR PACK
Lot codes and dates

191 of 191 products

Products covered by this recall
#BarcodesProduct as published
11019845930357940198459303570Lot Number: 22GBJ869; 2) DYNDA3188, UDI-DI: 10198459303579(each), 40198459303570(case)
21019845906545340198459065454Lot Number: 25DBF256; 3) DYNJG001027B, UDI-DI: 10198459065453(each), 40198459065454(case)
31019845906545340198459065454Lot Number: 25ELA998; 4) DYNJG001027B, UDI-DI: 10198459065453(each), 40198459065454(case)
41088438988205440884389882055Lot Number: 25ELA723; 5) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
51088438988205440884389882055Lot Number: 21BBH579; 6) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
61088438988205440884389882055Lot Number: 21BBS213; 7) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
71088438988205440884389882055Lot Number: 21DBS220; 8) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
81088438988205440884389882055Lot Number: 21HBK178; 9) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
91088438988205440884389882055Lot Number: 21IBV194; 10) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
101088438988205440884389882055Lot Number: 21JBJ063; 11) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
111088438988205440884389882055Lot Number: 21JBM583; 12) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
121088438988205440884389882055Lot Number: 22ABG678; 13) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
131088438988205440884389882055Lot Number: 22ABZ724; 14) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
141088438988205440884389882055Lot Number: 22DBL342; 15) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
151088438988205440884389882055Lot Number: 22IBS978; 16) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
161088438988205440884389882055Lot Number: 22JBV884; 17) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
171088438988205440884389882055Lot Number: 22LBH141; 18) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
181088438988205440884389882055Lot Number: 22OBE023; 19) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
191088438988205440884389882055Lot Number: 22OBE024; 20) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
201088438988205440884389882055Lot Number: 22OBE025; 21) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case)
Amount recalled
38014 units

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

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

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, 5:45 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.