FDA DeviceClass IINotable
FDA Recall: Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piec
Description
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Hazard
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Related Recalls
2026-08-12 · FDA_DEVICE
FDA Recall: Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO4010 Softw
TISSIUM SA
2026-08-12 · FDA_DEVICE
FDA Recall: 5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905
Aniara Diagnostica LLC
2026-08-12 · FDA_DEVICE
FDA Recall: Brand Name: Quantum Rehab Product Name: Quantum Outback Model/Catalog Number: Quantum Outback Sof
Pride Mobility Products Corp.
2026-08-12 · FDA_DEVICE
FDA Recall: STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
Stryker Corporation