Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026

Medline Convenience Kits

Medline Industries, LP

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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 Kits

22 of 22 products

Products covered by this recall
Model / numberProduct as published
CDS840144QOPEN HEART CDS
CDS840150WOPEN HEART
CDS840396AAOPEN HEART ADULT
CDS982269NCABG A CDS
CDS983849GOPEN HEART ANESTHESIA PACK
CDS984289LOPEN HEART ACCESSORY CDS
CDS985105QOPEN HEART A
DYNJ901075ROPEN HEART PART 2
DYNJ902664LVPH OPEN HEART
DYNJ903465IHEART A
DYNJ903822FHEART
DYNJ904311FOPEN HEART BASIC B
DYNJ904749JSM OPEN HEART PACK A&B
DYNJ905567BOPEN HEART ANESTHESIA ICC-B
DYNJ906102KSILVER CROSS OPEN HEART
DYNJ906225IANESTHESIA OPEN HEART
DYNJ907400FOPEN HEART COMBO
DYNJ908121CCARDIAC CABG B
DYNJ908308AFS OPEN HEART
DYNJ909116DOPEN HEART SUPPLEMENT
Lot codes and dates

284 of 284 products

Products covered by this recall
#BarcodesProduct as published
11019532726310240195327263103Lot Number: 24LBH805; 2) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
21019532726310240195327263103Lot Number: 24HBM100; 3) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
31019532726310240195327263103Lot Number: 25ABR195; 4) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
41019532726310240195327263103Lot Number: 25EBS810; 5) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
51019532726310240195327263103Lot Number: 25FBS936; 6) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
61019532726310240195327263103Lot Number: 25GBX096; 7) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
71019532726310240195327263103Lot Number: 25IBT859; 8) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case)
81019845956162740198459561628Lot Number: 24KBE879; 9) CDS840144R, UDI-DI: 10198459561627(each), 40198459561628(case)
91019845956162740198459561628Lot Number: 26DBF234; 10) CDS840144R, UDI-DI: 10198459561627(each), 40198459561628(case)
101019845956162740198459561628Lot Number: 26ABG176; 11) CDS840144R, UDI-DI: 10198459561627(each), 40198459561628(case)
111019532764804640195327648047Lot Number: 26ABK484; 12) CDS840150W, UDI-DI: 10195327648046(each), 40195327648047(case)
121019845911238640198459112387Lot Number: 24HBQ201; 13) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case)
131019845911238640198459112387Lot Number: 25CBD369; 14) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case)
141019845911238640198459112387Lot Number: 25DBL498; 15) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case)
151019845911238640198459112387Lot Number: 24LBD200; 16) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case)
161019845911238640198459112387Lot Number: 24LBD223; 17) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case)
171019845911238640198459112387Lot Number: 24LBR405; 18) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case)
181019845930302940198459303020Lot Number: 24JBX455; 19) CDS840150Y, UDI-DI: 10198459303029(each), 40198459303020(case)
191019845930302940198459303020Lot Number: 25FBD604; 20) CDS840150Y, UDI-DI: 10198459303029(each), 40198459303020(case)
201019845930302940198459303020Lot Number: 25FBT739; 21) CDS840150Y, UDI-DI: 10198459303029(each), 40198459303020(case)
Amount recalled
6775 units

This recall covers 20 products

The agency filed one notice per product. You are reading one of them; the other 19 are below.

7 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

Using this product could cause serious injury, illness or death — stop using it now.

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 (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 6:27 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.