Reported Jul 26, 2023 · Ongoing

Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following

MEDLINE INDUSTRIES, LP - Northfield

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 - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following

26 of 26 products

Products covered by this recall
Model / numberProduct as published
DYNJ67770AEP PACER PACK
DYNJ67771EP PROCEDURE PACK
DYNJ68019EP PACK
DYNJ68198GWINNETT ENDOVASCULAR WSTE MGT
DYNJ68499BTAVR PACK
DYNJ68667VEIN CLINIC
DYNJ68863VASCULAR PACK
DYNJ68880VASCULAR PACK
DYNJ68933TAVR PACK
DYNJ68968APROCEDURE PACK
DYNJ68990APORT PACK
DYNJ69009ASTROKE PACK
DYNJ69108AENDOVENOUS BASIC PACK
DYNJ69272AVEIN ABLATION KIT
DYNJ69302UPPER ENDOVASCULAR PK
DYNJ69422STROKE PACK
DYNJ69622UNM PREHOSPITAL ECMO PACK
DYNJ69624UNM ACCESS PACK
DYNJ69626FLUSHING VASCULAR CENTER
DYNJ69682AFIB PACK
Lot codes and dates

26 of 26 products

Products covered by this recall
#BarcodesProduct as published
11019532729097940195327290970Model Numbers DYNJ67770A, UDI/DI (EA)10195327290979, UDI/DI (CS)40195327290970
21019348943072140193489430722Model Numbers DYNJ67771, UDI/DI (EA)10193489430721, UDI/DI (CS)40193489430722
31019348946784040193489467841Model Numbers DYNJ68019, UDI/DI (EA)10193489467840, UDI/DI (CS)40193489467841
41019348949917940193489499170Model Numbers DYNJ68198, UDI/DI (EA)10193489499179, UDI/DI (CS)40193489499170
51019532703405440195327034055Model Numbers DYNJ68499B, UDI/DI (EA)10195327034054, UDI/DI (CS)40195327034055
61019348983731540193489837316Model Numbers DYNJ68667, UDI/DI (EA)10193489837315, UDI/DI (CS)40193489837316
71019348984540240193489845403Model Numbers DYNJ68863, UDI/DI (EA)10193489845402, UDI/DI (CS)40193489845403
81019348984772740193489847728Model Numbers DYNJ68880, UDI/DI (EA)10193489847727, UDI/DI (CS)40193489847728
91019348986037540193489860376Model Numbers DYNJ68933, UDI/DI (EA)10193489860375, UDI/DI (CS)40193489860376
101019532720684040195327206841Model Numbers DYNJ68968A, UDI/DI (EA)10195327206840, UDI/DI (CS)40195327206841
111019348998136040193489981361Model Numbers DYNJ68990A, UDI/DI (EA)10193489981360, UDI/DI (CS)40193489981361
121019532707556940195327075560Model Numbers DYNJ69009A, UDI/DI (EA)10195327075569, UDI/DI (CS)40195327075560
131019532702571740195327025718Model Numbers DYNJ69108A, UDI/DI (EA)10195327025717, UDI/DI (CS)40195327025718
141019532701580040195327015801Model Numbers DYNJ69272A, UDI/DI (EA)10195327015800, UDI/DI (CS)40195327015801
151019348992627940193489926270Model Numbers DYNJ69302, UDI/DI (EA)10193489926279, UDI/DI (CS)40193489926270
161019348993754140193489937542Model Numbers DYNJ69422, UDI/DI (EA)10193489937541, UDI/DI (CS)40193489937542
171019348995958140193489959582Model Numbers DYNJ69622, UDI/DI (EA)10193489959581, UDI/DI (CS)40193489959582
181019348995956740193489959568Model Numbers DYNJ69624, UDI/DI (EA)10193489959567, UDI/DI (CS)40193489959568
191019348996069340193489960694Model Numbers DYNJ69626, UDI/DI (EA)10193489960693, UDI/DI (CS)40193489960694
201019348996892740193489968928Model Numbers DYNJ69682, UDI/DI (EA)10193489968927, UDI/DI (CS)40193489968928
Amount recalled
# included in 3,740,814 units total

This recall covers 53 products

The agency filed one notice per product. You are reading one of them; the other 52 are below.

40 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

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, 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.