💊 Drugs Class I - Dangerous
Chemical Contamination: Presence of Undeclared Methanol
All Recalls
95,114 total recalls in our database
💊 Drugs Class I - Dangerous
Incorrect/Undeclared Excipients: Notification received from Health Canada that DA-2I Ethanol is a type not an approved for use in Hand Sanitizer.
🏥 Medical Devices Class I - Dangerous
The needle surface deteriorated due to unexpected electrolysis during procedure.
🏥 Medical Devices Class I - Dangerous
The needle surface deteriorated due to unexpected electrolysis during procedure.
Safe-T PLUS Thora-Para 5 Fr Catheter Drainage Tray
Carefusion 2200
🏥 Medical Devices Class I - Dangerous
The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
🏥 Medical Devices Class I - Dangerous
The needle surface deteriorated due to unexpected electrolysis during procedure.
SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number CPA00040 (UDI 00801741143892)
Becton Dickinson & Company
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers PA-0031G (UDI 00801741085666), PA-0031YNG (UDI 00801741085673), PA-0032G (UDI 00801741087639), PA-0033G (UDI 00801741096433)
Becton Dickinson & Company
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
LoFric Origo, Tiemann, 16in, FR12 urinary catheters
Wellspect HealthCare (Division of DENTSPLY IH AB)
🏥 Medical Devices Class I - Dangerous
Wellspect Healthcare is voluntarily recalling certain LoFric¿ Origo" urethral catheters due to a potential defect which may be present in the catheters distal tip.
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224)
Becton Dickinson & Company
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
🏥 Medical Devices Class I - Dangerous
Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.
🏥 Medical Devices Class I - Dangerous
A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve.
🏥 Medical Devices Class I - Dangerous
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
🏥 Medical Devices Class I - Dangerous
6.0x50mm poly-reduction screws were laser etched 6.0x45
Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray
Carefusion 2200
🏥 Medical Devices Class I - Dangerous
The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.
🏥 Medical Devices Class I - Dangerous
Insufficient amount of antibody without an error message or alarm