FDA DeviceClass INotable
FDA Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syring
Description
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Hazard
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Remedy
2154 units
Related Recalls
2026-06-03 · FDA_DEVICE
FDA Recall: Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPI
Medline Industries, LP
2026-06-03 · FDA_DEVICE
FDA Recall: Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BL
Medline Industries, LP
2026-06-03 · FDA_DEVICE
FDA Recall: Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOC
Medline Industries, LP
2026-06-03 · FDA_DEVICE
FDA Recall: Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL
Medline Industries, LP