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
12 of 12 products
| Model / number | Product as published |
|---|---|
DYNJQ0505M | ANGIOGRAPHY PACK-LF |
DYNJT2021G | ANGIO PACK |
DYNJ31377B | ANGIOGRAPHY PACK |
DYNJ51279 | ANGIO PACK |
DYNJ52447 | ANGIOGRAPHY PACK II |
DYNJ53369C | CATH ANGIO PACK |
DYNJ53591A | ANGIO PACK |
DYNJ57516 | ANGIOGRAPHIC PACK |
DYNJ58722A | ANGIOGRAPHY TRAY-LF |
DYNJ62742 | ANGIO TRAY W/CHLORAPREP |
DYNJ67876 | CEREBRAL ANGIOGRAM |
VASC1170A | CSU CATH MANIFOLD KIT |
- Lot codes and dates
33 of 33 products
Products covered by this recall # Barcodes Product as published 1 1088994284690040889942846901Lot Number: 23KBL880; 2) DYNJQ0505M, UDI-DI: 10889942846900(each), 40889942846901(case) 2 1088994284690040889942846901Lot Number: 24ABA125; 3) DYNJQ0505M, UDI-DI: 10889942846900(each), 40889942846901(case) 3 1019348960881640193489608817Lot Number: 23IBA898; 4) DYNJT2021G, UDI-DI: 10193489608816(each), 40193489608817(case) 4 1088994210669140889942106692Lot Number: 24CMH245; 5) DYNJ31377B, UDI-DI: 10889942106691(each), 40889942106692(case) 5 1088994210669140889942106692Lot Number: 25LBQ639; 6) DYNJ31377B, UDI-DI: 10889942106691(each), 40889942106692(case) 6 1088994214530040889942145301Lot Number: 25GBF384; 7) DYNJ51279, UDI-DI: 10889942145300(each), 40889942145301(case) 7 1088994214530040889942145301Lot Number: 25DBQ486; 8) DYNJ51279, UDI-DI: 10889942145300(each), 40889942145301(case) 8 1088994227977740889942279778Lot Number: 25CBT538; 9) DYNJ52447, UDI-DI: 10889942279777(each), 40889942279778(case) 9 1019348965133140193489651332Lot Number: 25FMA232; 10) DYNJ53369C, UDI-DI: 10193489651331(each), 40193489651332(case) 10 1019348965133140193489651332Lot Number: 25ILA917; 11) DYNJ53369C, UDI-DI: 10193489651331(each), 40193489651332(case) 11 1088994259237140889942592372Lot Number: 25FLA554; 12) DYNJ53591A, UDI-DI: 10889942592371(each), 40889942592372(case) 12 1088994274842640889942748427Lot Number: 25FBA222; 13) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 13 1088994274842640889942748427Lot Number: 21JBN533; 14) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 14 1088994274842640889942748427Lot Number: 21KBM563; 15) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 15 1088994274842640889942748427Lot Number: 21KBQ110; 16) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 16 1088994274842640889942748427Lot Number: 21LBI454; 17) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 17 1088994274842640889942748427Lot Number: 23DMF559; 18) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 18 1088994274842640889942748427Lot Number: 23EMB053; 19) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 19 1088994274842640889942748427Lot Number: 23FME913; 20) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) 20 1088994274842640889942748427Lot Number: 23JME012; 21) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case) - Amount recalled
- 3183 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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