FDA DeviceClass IINotable
FDA Recall: Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257F
Description
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Hazard
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Remedy
6 units
Related Recalls
2026-07-29 · FDA_DEVICE
FDA Recall: Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc ba
Medline Industries, LP
2026-07-29 · FDA_DEVICE
FDA Recall: Medline medical convenience kits labeled as: 1) SHOULDER PACK, Medline Kit SKU DYNJ39590O; 2) S
Medline Industries, LP
2026-07-29 · FDA_DEVICE
FDA Recall: MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
Medline Industries, LP
2026-07-29 · FDA_DEVICE
FDA Recall: Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU DYNJ65065A: 2)
Medline Industries, LP