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

Products covered by this recall
Model / numberProduct as published
DYNJQ0505MANGIOGRAPHY PACK-LF
DYNJT2021GANGIO PACK
DYNJ31377BANGIOGRAPHY PACK
DYNJ51279ANGIO PACK
DYNJ52447ANGIOGRAPHY PACK II
DYNJ53369CCATH ANGIO PACK
DYNJ53591AANGIO PACK
DYNJ57516ANGIOGRAPHIC PACK
DYNJ58722AANGIOGRAPHY TRAY-LF
DYNJ62742ANGIO TRAY W/CHLORAPREP
DYNJ67876CEREBRAL ANGIOGRAM
VASC1170ACSU CATH MANIFOLD KIT
Lot codes and dates

33 of 33 products

Products covered by this recall
#BarcodesProduct as published
11088994284690040889942846901Lot Number: 23KBL880; 2) DYNJQ0505M, UDI-DI: 10889942846900(each), 40889942846901(case)
21088994284690040889942846901Lot Number: 24ABA125; 3) DYNJQ0505M, UDI-DI: 10889942846900(each), 40889942846901(case)
31019348960881640193489608817Lot Number: 23IBA898; 4) DYNJT2021G, UDI-DI: 10193489608816(each), 40193489608817(case)
41088994210669140889942106692Lot Number: 24CMH245; 5) DYNJ31377B, UDI-DI: 10889942106691(each), 40889942106692(case)
51088994210669140889942106692Lot Number: 25LBQ639; 6) DYNJ31377B, UDI-DI: 10889942106691(each), 40889942106692(case)
61088994214530040889942145301Lot Number: 25GBF384; 7) DYNJ51279, UDI-DI: 10889942145300(each), 40889942145301(case)
71088994214530040889942145301Lot Number: 25DBQ486; 8) DYNJ51279, UDI-DI: 10889942145300(each), 40889942145301(case)
81088994227977740889942279778Lot Number: 25CBT538; 9) DYNJ52447, UDI-DI: 10889942279777(each), 40889942279778(case)
91019348965133140193489651332Lot Number: 25FMA232; 10) DYNJ53369C, UDI-DI: 10193489651331(each), 40193489651332(case)
101019348965133140193489651332Lot Number: 25ILA917; 11) DYNJ53369C, UDI-DI: 10193489651331(each), 40193489651332(case)
111088994259237140889942592372Lot Number: 25FLA554; 12) DYNJ53591A, UDI-DI: 10889942592371(each), 40889942592372(case)
121088994274842640889942748427Lot Number: 25FBA222; 13) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
131088994274842640889942748427Lot Number: 21JBN533; 14) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
141088994274842640889942748427Lot Number: 21KBM563; 15) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
151088994274842640889942748427Lot Number: 21KBQ110; 16) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
161088994274842640889942748427Lot Number: 21LBI454; 17) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
171088994274842640889942748427Lot Number: 23DMF559; 18) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
181088994274842640889942748427Lot Number: 23EMB053; 19) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
191088994274842640889942748427Lot Number: 23FME913; 20) DYNJ57516, UDI-DI: 10889942748426(each), 40889942748427(case)
201088994274842640889942748427Lot 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:55 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.