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
6 of 6 products
| Model / number | Product as published |
|---|---|
DYNJ07425 | ARTHROGRAM TRAY |
DYNJ38610I | TOL NEURO ANGIO PACK |
DYNJ45234A | ANGIOGRAPHY PACK |
DYNJ53064B | C.I.C.N. ANGIO PACK |
DYNJ63779A | DR. ALLEYNE NEURO PACK |
DYNJ87817 | NEURO CTM IR PACK |
- Lot codes and dates
15 of 15 products
Products covered by this recall # Barcodes Product as published 1 1008019686646540080196866466Lot Number: 23DBP927; 2) DYNJ07425, UDI-DI: 10080196866465(each), 40080196866466(case) 2 1019845932310240198459323103Lot Number: 23EBS362; 3) DYNJ38610I, UDI-DI: 10198459323102(each), 40198459323103(case) 3 1019845932310240198459323103Lot Number: 25DBM593; 4) DYNJ38610I, UDI-DI: 10198459323102(each), 40198459323103(case) 4 1019348978255440193489782555Lot Number: 25GBO740; 5) DYNJ45234A, UDI-DI: 10193489782554(each), 40193489782555(case) 5 1019348978255440193489782555Lot Number: 23LBU617; 6) DYNJ45234A, UDI-DI: 10193489782554(each), 40193489782555(case) 6 1019348978916440193489789165Lot Number: 23HBK865; 7) DYNJ53064B, UDI-DI: 10193489789164(each), 40193489789165(case) 7 1019348978916440193489789165Lot Number: 24BMC721; 8) DYNJ53064B, UDI-DI: 10193489789164(each), 40193489789165(case) 8 1019348978916440193489789165Lot Number: 24EMF715; 9) DYNJ53064B, UDI-DI: 10193489789164(each), 40193489789165(case) 9 1019348935584040193489355841Lot Number: 24AMI140; 10) DYNJ63779A, UDI-DI: 10193489355840(each), 40193489355841(case) 10 1019845906918540198459069186Lot Number: 25HBM008; 11) DYNJ87817, UDI-DI: 10198459069185(each), 40198459069186(case) 11 1019845906918540198459069186Lot Number: 24HBF527; 12) DYNJ87817, UDI-DI: 10198459069185(each), 40198459069186(case) 12 1019845906918540198459069186Lot Number: 25BBL663; 13) DYNJ87817, UDI-DI: 10198459069185(each), 40198459069186(case) 13 1019845906918540198459069186Lot Number: 25CBN143; 14) DYNJ87817, UDI-DI: 10198459069185(each), 40198459069186(case) 14 1019845906918540198459069186Lot Number: 25EBJ520; 15) DYNJ87817, UDI-DI: 10198459069185(each), 40198459069186(case) 15 Lot Number: 25FBC657 - Amount recalled
- 9645 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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