Official recall notice

FDA DeviceClass IINotable

FDA Recall: Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION,

Recall date
2026-09-02
FDA class
Class II

Why it was recalled

Hazard

Kits contain a potentially contaminated component which were recalled by the manufacturer

Product description

Kits contain a potentially contaminated component which were recalled by the manufacturer

Affected products

Medline Kit SKU DYNJ904612L, UDI/DI 10198459495625 (each) 40198459495626 (case), Lot Number 26FMC710; Medline Kit SKU DYNJ904612L, UDI/DI 10198459495625 (each) 40198459495626 (case), Lot Number 26DMG417; Medline Kit SKU DYNJ911755, UDI/DI 10198459523946 (each) 40198459523947 (case), Lot Number 25KMI628; Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) 40198459599560 (case), Lot Number 26ABJ549; Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) 40198459599560 (case), Lot Number 26ABI899; Medline Kit SKU DYNJ912014, UDI/DI 10198459599569 (each) 40198459599560 (case), Lot Number 25LBT433.

Verify with the official notice →
Share:

Related Recalls

2026-09-09 · FDA_DEVICE
FDA Recall: Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT ADMIN KIT DY
Medline Industries, LP
2026-09-09 · FDA_DEVICE
FDA Recall: Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A
Medline Industries, LP
2026-09-09 · FDA_DEVICE
FDA Recall: Medline Convenience Kits: 1) IV START KIT LAB DRAW-SH, Model Number: CDS860014P; 2) IV START KIT,
Medline Industries, LP
2026-09-09 · FDA_DEVICE
FDA Recall: Medline Convenience Kits: 1) PRE-OP KIT, Catalog Number: DYKS1043F; 2) PRE OP KIT, Catalog Number
Medline Industries, LP