Medline Industries, Lp: Orthopedic Tray

Recall Summary Medline Industries is recalling four orthopedic surgery kits (used for spine fusion, neurosurgery, and craniotomy procedures) because they contain a potentially contaminated component supplied by the manufacturer. These kits were distributed nationwide to hospitals and medical facilities. This is a Class I recall, the most serious classification.

Recalling firm
Medline Industries, LP
Product
Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.
Reason
Kits contain a potentially contaminated component which were recalled by the manufacturer
Classification
Class I
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-07-10
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fc5cc5ec-da82-444a-986f-3911e1bdbe43