Medline Industries, LP
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Kits contain a potentially contaminated component which were recalled by the manufacturer
Medline convenience kits labeled as: 1) LAVH, Medline Kit SKU CDS982273U; 2) GYN ABDOMINAL CDS, Medline Kit SKU CDS982654L; 3) GYN LAP HYSTERECTOMY CDS, Medline Kit SKU CDS982662Q; 4) CMH VAG HYSTERECTOMY PK-LF, Medline Kit SKU DYNJ54382F; 5) A P RESECTION, Medline Kit SKU DYNJ903467L.
Medline Kit SKU CDS982273U, UDI/DI 10198459385827 (each) 40198459385828 (case), Lot Number 25LBR956; Medline Kit SKU CDS982273U, UDI/DI 10198459385827 (each) 40198459385828 (case), Lot Number 25KBP729; Medline Kit SKU CDS982654L, UDI/DI 10195327306830 (each) 40195327306831 (case), Lot Number 26EBN087; Medline Kit SKU CDS982662Q, UDI/DI 10195327306793 (each) 40195327306794 (case), Lot Number 25JBK543; Medline Kit SKU DYNJ54382F, UDI/DI 10198459794285 (each) 40198459794286 (case), Lot Number 26FMC227; Medline Kit SKU DYNJ903467L, UDI/DI 10198459293207 (each) 40198459293208 (case), Lot Number 26DMK551; Medline Kit SKU DYNJ903467L, UDI/DI 10198459293207 (each) 40198459293208 (case), Lot Number 26DMB880.
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →