Lower risk Medical device recall · FDA · Published June 8, 2026

Medline Medical Procedure Kits Recalled for Possible Drug Ineffectiveness

Medline recalls specific knee and hip procedure kits due to quality issues with pain management drugs that may not work as intended.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2765-2026Medical device Medline ›

Lower-risk recall

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.

✎ GovInfoNow plain-language explainer

Medline is recalling several medical procedure kits for knee and hip surgeries because the pain management drugs inside could be ineffective due to quality issues. This means the kits might not provide the intended pain relief during surgery. Read more at govinfonow.com/recall/127815-medline-medical-procedure-kits-recalled-for-possible-drug-ineffectiveness.

Source Summary by GovInfoNow · govinfonow.com/recall/127815-medline-medical-procedure-kits-recalled-for-possible-drug-ineffectiveness · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2765-2026

Cite this page

“Medline Medical Procedure Kits Recalled for Possible Drug Ineffectiveness.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/127815-medline-medical-procedure-kits-recalled-for-possible-drug-ineffectiveness. Based on FDA recall #Z-2765-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2765-2026%22&limit=1).

The FDA announced on June 8, 2026, that Medline Industries, LP is recalling medical procedure convenience kits due to quality issues in included pain management kits that could result in drug ineffectiveness. According to the FDA, the recall involves specific SKUs and lot codes distributed in Missouri, Colorado, and Illinois.

How to tell if you have it

Brand: Medline
Product: MEDLINE medical procedure convenience kit labeled as TOTAL KNEE-LF (SKU CDSOPT590T)
Product: TOTAL KNEE-LF (SKU CDSOPT590U)
Product: TOTAL KNEE CDS (SKU CDS983930J)
Product: HIP CDS-LF (SKU CDS984556L)
Product: HIP CDS-LF (SKU CDS984556M)
Product: TOTAL KNEE PACK (SKU DYNJ905162Q)
Lot Numbers: 24GDA740, 26EDA279, 26BDB734, 26ADA474, 25LDA001, 25KDB325, 25GDB517, 25FDB017, 25DDA155, 24LDA248, 25KBL209, 24JDC180, 24HDA321, 25ADB327, 26CBD346, 25KBU219

The hazard

The recalled procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP. These components were previously recalled due to quality issues that could result in drug ineffectiveness.

Context

GovInfoNow's records show Medline Industries, LP has had 68 other recalls on record since July 31, 2025. Other recent recalls of similar products include Medline Basic Homecare Beds and Medlite Homecare Beds (August 14, 2026), Medline Convenience Kits (August 11, 2026), and Medline convenience kits containing Healthmark Instrument Channel Brushes (August 10, 2026). Other recent recalls of similar products include B Braun Medical Spinal Needle Kits (May 6, 2026), Braun Medical Spinal Needle Kits (May 6, 2026), and B Braun Spinocan Spinal Needle Kits (May 6, 2026).

How to tell if you have this one

Check for Medline kits labeled as TOTAL KNEE-LF (SKUs CDSOPT590T/U), TOTAL KNEE CDS (SKU CDS983930J), HIP CDS-LF (SKUs CDS984556L/M), or TOTAL KNEE PACK (SKU DYNJ905162Q). Look for specific lot numbers and UDI/DI codes listed in the recall notice.

Brand
Medline
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class I
Status
Ongoing
Distribution
US: Mo, CO, IL

Recall number	Product, codes & lots	Quantity
Z-2764-2026	MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N; UDI/DI 10198459266621 (each) 40198459266622 (case), Lot Numbers: 26EDA285, 26DDA718, 26BDB740, 26ADB079, 26ADA161, 25KDB472, 25GDA213.	52 kits
Z-2765-2026	MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF, Medline kit SKU CDSOPT590T; 2) TOTAL KNEE-LF, Medline kit SKU CDSOPT590U; 3) TOTAL KNEE CDS, Medline kit SKU CDS983930J; 4) HIP CDS-LF, Medline kit SKU CDS984556L; 5) HIP CDS-LF, Medline kit SKU CDS984556M; 6) TOTAL KNEE PACK, Medline kit SKU DYNJ905162Q.; Medline kit SKU CDSOPT590T, UDI/DI 10195327555009 (each) 40195327555000 (case), Kit Lot Number 24GDA740; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 26EDA279; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 26BDB734; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 26ADA474; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25LDA001; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25KDB325; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25GDB517; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25FDB017; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 25DDA155; Medline kit SKU CDSOPT590U, UDI/DI 10198459180255 (each) 40198459180256 (case), Kit Lot Number 24LDA248; Medline kit SKU CDS983930J, UDI/DI 10193489512298 (each) 40193489512299 (case), Kit Lot Number 25KBL209; Medline kit SKU CDS984556L, UDI/DI 10195327554996 (each) 40195327554997 (case), Kit Lot Number 24JDC180; Medline kit SKU CDS984556L, UDI/DI 10195327554996 (each) 40195327554997 (case), Kit Lot Number 24HDA321; Medline kit SKU CDS984556M, UDI/DI 10198459180248 (each) 40198459180249 (case), Kit Lot Number 25ADB327; Medline kit SKU DYNJ905162Q, UDI/DI 10198459235900 (each) 40198459235901 (case), Kit Lot Number 26CBD346; Medline kit SKU DYNJ905162Q, UDI/DI 10198459235900 (each) 40198459235901 (case), Kit Lot Number 25KBU219.	318 kits

Based on the official FDA remedy

What to do — step by step

Check Kit Details
Review the product label for the specific SKU and lot number to confirm if your kit is affected.

Where it went and when

Where it was distributed

Distributed in 3 states.

FDA distribution: “US: Mo, CO, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado, Illinois, Missouri.

Recall timeline

FDA published this recall 51 days after the firm started it.

Jun 8, 2026Firm started the recall
Jul 22, 2026FDA classified it Class I
Jul 29, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest medical device recalls

Keep exploring

More Medline recalls

Link to this recall

<a href="https://govinfonow.com/recall/127815-medline-medical-procedure-kits-recalled-for-possible-drug-ineffectiveness">Medline Medical Procedure Kits Recalled for Possible Drug Ineffectiveness (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2765-2026 (June 8, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2765-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.