HIGHFDA DEVICE

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; ...

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.

Medline Industries, LPHealth & Personal CareMedical DevicesMedline kit SKU CDSOPT590TUDI/DI 10195327555009 (each) 40195327555000 (case)Kit Lot Number 24GDA740

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
June 8, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
June 8, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Geographic Scope
2 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Model numbers
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, Kit Lot Number 26BDB734, Kit Lot Number 26ADA474 +2 more
Where affected
CO, IL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    June 8, 2026

  2. Reported by FDA DEVICE

    July 29, 2026

  3. RecallRadar source check

    August 4, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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Full Description

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.. Reason: 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.. Classification: Class I. Quantity: 318 kits. Distribution: US: Mo, CO, IL

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Medline kit SKU CDSOPT590T
UDI/DI 10195327555009 (each) 40195327555000 (case)
Kit Lot Number 24GDA740
Medline kit SKU CDSOPT590U
UDI/DI 10198459180255 (each) 40198459180256 (case)
+5 more
Affected States
CO, IL
Report Date
July 29, 2026
Recall Status
ACTIVE

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