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
| Model / number | Product as published |
|---|---|
CDS840144Q | OPEN HEART CDS |
CDS840150W | OPEN HEART |
CDS840396AA | OPEN HEART ADULT |
CDS982269N | CABG A CDS |
CDS983849G | OPEN HEART ANESTHESIA PACK |
CDS984289L | OPEN HEART ACCESSORY CDS |
CDS985105Q | OPEN HEART A |
DYNJ901075R | OPEN HEART PART 2 |
DYNJ902664L | VPH OPEN HEART |
DYNJ903465I | HEART A |
DYNJ903822F | HEART |
DYNJ904311F | OPEN HEART BASIC B |
DYNJ904749J | SM OPEN HEART PACK A&B |
DYNJ905567B | OPEN HEART ANESTHESIA ICC-B |
DYNJ906102K | SILVER CROSS OPEN HEART |
DYNJ906225I | ANESTHESIA OPEN HEART |
DYNJ907400F | OPEN HEART COMBO |
DYNJ908121C | CARDIAC CABG B |
DYNJ908308A | FS OPEN HEART |
DYNJ909116D | OPEN HEART SUPPLEMENT |
- Lot codes and dates
284 of 284 products
Products covered by this recall # Barcodes Product as published 1 1019532726310240195327263103Lot Number: 24LBH805; 2) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 2 1019532726310240195327263103Lot Number: 24HBM100; 3) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 3 1019532726310240195327263103Lot Number: 25ABR195; 4) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 4 1019532726310240195327263103Lot Number: 25EBS810; 5) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 5 1019532726310240195327263103Lot Number: 25FBS936; 6) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 6 1019532726310240195327263103Lot Number: 25GBX096; 7) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 7 1019532726310240195327263103Lot Number: 25IBT859; 8) CDS840144Q, UDI-DI: 10195327263102(each), 40195327263103(case) 8 1019845956162740198459561628Lot Number: 24KBE879; 9) CDS840144R, UDI-DI: 10198459561627(each), 40198459561628(case) 9 1019845956162740198459561628Lot Number: 26DBF234; 10) CDS840144R, UDI-DI: 10198459561627(each), 40198459561628(case) 10 1019845956162740198459561628Lot Number: 26ABG176; 11) CDS840144R, UDI-DI: 10198459561627(each), 40198459561628(case) 11 1019532764804640195327648047Lot Number: 26ABK484; 12) CDS840150W, UDI-DI: 10195327648046(each), 40195327648047(case) 12 1019845911238640198459112387Lot Number: 24HBQ201; 13) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case) 13 1019845911238640198459112387Lot Number: 25CBD369; 14) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case) 14 1019845911238640198459112387Lot Number: 25DBL498; 15) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case) 15 1019845911238640198459112387Lot Number: 24LBD200; 16) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case) 16 1019845911238640198459112387Lot Number: 24LBD223; 17) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case) 17 1019845911238640198459112387Lot Number: 24LBR405; 18) CDS840150X, UDI-DI: 10198459112386(each), 40198459112387(case) 18 1019845930302940198459303020Lot Number: 24JBX455; 19) CDS840150Y, UDI-DI: 10198459303029(each), 40198459303020(case) 19 1019845930302940198459303020Lot Number: 25FBD604; 20) CDS840150Y, UDI-DI: 10198459303029(each), 40198459303020(case) 20 1019845930302940198459303020Lot 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.
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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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