Medline Industries, Lp: Orthopedic Tray

Recall Summary Medline is recalling six orthopedic procedure kits used in knee and hip surgeries because they contain pain management medication (Bupivacaine Hydrochloride in Dextrose Injection) with quality issues that may make the drug ineffective. The affected kits were distributed to medical facilities in Colorado, Illinois, and Missouri. This is a Class I recall, the most serious classification.

Recalling firm
Medline Industries, LP
Product
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
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-06-08
Status
Open, Classified
Areas affected
CO, IL, MO
Distribution
US: Mo, CO, IL

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f1867911-6e97-438c-b69b-7f05e802bf1a