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
| Model / number | Product as published |
|---|---|
DYKB1038 | NEWBORN ADMISSION |
DYNDA3188 | DRAINAGE TRAY |
DYNJG001027B | VA ORLANDO SHOULDER PACK |
| — | TUMESCENT SYRINGE KIT, Model Number: DYNJTUMSYR |
DYNJT3719 | OMC PTCA PACK |
DYNJT5667 | PORT PACK |
DYNJWASTEKIT2 | WASTE MANAGEMENT KIT - 2 |
DYNJ20175J | CARDIAC CATH |
DYNJ33521D | D&C PACK-POB |
DYNJ38533F | BASIC PACK |
DYNJ39230D | CATH PACK IMPLANT |
DYNJ40886B | CERVICAL SPINE PACK |
DYNJ41553F | MV-IR ANGIO DRAPE PACK-LF |
DYNJ41558D | TV ENDOVASCULAR-LF |
DYNJ44816J | MAJOR PACK-LF |
DYNJ48683A | ANGIOGRAPHY PACK |
DYNJ55922C | EXTREMITY PACK |
DYNJ57785C | NEURO PACK |
DYNJ61377B | PACEMAKER PACK |
DYNJ62683D | VASCULAR PACK |
- Lot codes and dates
191 of 191 products
Products covered by this recall # Barcodes Product as published 1 1019845930357940198459303570Lot Number: 22GBJ869; 2) DYNDA3188, UDI-DI: 10198459303579(each), 40198459303570(case) 2 1019845906545340198459065454Lot Number: 25DBF256; 3) DYNJG001027B, UDI-DI: 10198459065453(each), 40198459065454(case) 3 1019845906545340198459065454Lot Number: 25ELA998; 4) DYNJG001027B, UDI-DI: 10198459065453(each), 40198459065454(case) 4 1088438988205440884389882055Lot Number: 25ELA723; 5) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 5 1088438988205440884389882055Lot Number: 21BBH579; 6) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 6 1088438988205440884389882055Lot Number: 21BBS213; 7) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 7 1088438988205440884389882055Lot Number: 21DBS220; 8) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 8 1088438988205440884389882055Lot Number: 21HBK178; 9) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 9 1088438988205440884389882055Lot Number: 21IBV194; 10) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 10 1088438988205440884389882055Lot Number: 21JBJ063; 11) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 11 1088438988205440884389882055Lot Number: 21JBM583; 12) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 12 1088438988205440884389882055Lot Number: 22ABG678; 13) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 13 1088438988205440884389882055Lot Number: 22ABZ724; 14) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 14 1088438988205440884389882055Lot Number: 22DBL342; 15) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 15 1088438988205440884389882055Lot Number: 22IBS978; 16) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 16 1088438988205440884389882055Lot Number: 22JBV884; 17) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 17 1088438988205440884389882055Lot Number: 22LBH141; 18) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 18 1088438988205440884389882055Lot Number: 22OBE023; 19) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 19 1088438988205440884389882055Lot Number: 22OBE024; 20) DYNJTUMSYR, UDI-DI: 10884389882054(each), 40884389882055(case) 20 1088438988205440884389882055Lot 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.
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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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