Reported Jun 24, 2026 · Ongoing

Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK…

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 convenience kitsBIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MRNGSD DYNJ58354F PACEMAKER PACK-LF DYNJ0618174N PACEMAKER SETUP PACK DYNJ35761D PACER / CATH LAB PACK-LF DYNJ0972604A PACER CDS CDS983686I PACER PACK DYNJ52059D PK, EP LAB PACEMAKER DYNJ43663A VENOUS ACCESS PACK DYNJ45640B
Lot codes and dates

12 of 12 products

Products covered by this recall
#BarcodesProduct as published
110193489903669Lot 25LBP470 DYNJ56573B UDI-DI 10193489903669
210195327674755Lot 25KBK220 DYNJ29135N UDI-DI 10195327674755
3101934899020441019845914913910195327104542Lot 25LMG563 DYNJ65916B UDI-DI 10193489902044 Lots 25KBG852 25LBB895 CDS983672P UDI-DI 10198459149139 Lots 25LBO027 26BBB852 DYNJ21877W UDI-DI 10195327104542
410198459224447Lot 25JBW040 DYNJ39316D UDI-DI 10198459224447
510195327515232Lot 25KBH774 DYNJ58354F UDI-DI 10195327515232
610195327227340Lot 25KBI240 DYNJ0618174N UDI-DI 10195327227340
710195327565374Lot 25KBC715 DYNJ35761D UDI-DI 10195327565374
810889942403905Lot 26CBC772 DYNJ0972604A UDI-DI 10889942403905
910193489852981Lot 25LMF965 CDS983686I UDI-DI 10193489852981
101019532736178510193489793680Lot 26ABE755 DYNJ52059D UDI-DI 10195327361785 Lots 25LBQ917 26CBE736 DYNJ43663A UDI-DI 10193489793680
1110193489494983Lot 26CBB662 DYNJ45640B UDI-DI 10193489494983
12Lot 25LMJ305
Amount recalled
49,654 kits total

This recall covers 64 products

The agency filed one notice per product. You are reading one of them; the other 63 are below.

51 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

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, 6:54 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.