Reported Jul 29, 2026 · Ongoing · Updated Sep 16, 2026
MEDLINE medical procedure convenience kit labeled as
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?
16 of 16 products
| Model / number | Barcodes | Product as published |
|---|---|---|
CDSOPT590T | 1019532755500940195327555000 | Medline kit , UDI/DI 10195327555009 (each) 40195327555000 (case), Kit Lot Number 24GDA740 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 26EDA279 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 26BDB734 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 26ADA474 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25LDA001 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25KDB325 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25GDB517 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25FDB017 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25DDA155 |
CDSOPT590U | 1019845918025540198459180256 | Medline kit , UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 24LDA248 |
CDS983930J | 1019348951229840193489512299 | Medline kit , UDI/DI 10193489512298 (each) 40193489512299 (case), Kit Lot Number 25KBL209 |
CDS984556L | 1019532755499640195327554997 | Medline kit , UDI/DI 10195327554996 (each) 40195327554997 (case), Kit Lot Number 24JDC180 |
CDS984556L | 1019532755499640195327554997 | Medline kit , UDI/DI 10195327554996 (each) 40195327554997 (case), Kit Lot Number 24HDA321 |
CDS984556M | 1019845918024840198459180249 | Medline kit , UDI/DI 10198459180248 (each) 40198459180249 (case), Kit Lot Number 25ADB327 |
DYNJ905162Q | 1019845923590040198459235901 | Medline kit , UDI/DI 10198459235900 (each) 40198459235901 (case), Kit Lot Number 26CBD346 |
DYNJ905162Q | 1019845923590040198459235901 | Medline kit , UDI/DI 10198459235900 (each) 40198459235901 (case), Kit Lot Number 25KBU219. |
- Amount recalled
- 318 kits
This recall covers 18 products
The agency filed one notice per product. You are reading one of them; the other 17 are below.
5 more are in the archive.
Where it was sold
Why it was recalled
Stop using this product now
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness.
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.
Free recall alerts
Get alerted about new Medline Industries, LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.