🏥 Medical Devices Class I - Dangerous
Breaking at the point of a welded joint
All Recalls
95,025 total recalls in our database
🏥 Medical Devices Class I - Dangerous
A recent FDA inspection at the firm identified that the foil test performed during installation of the device does not have clear acceptance criteria.
Moravian Star lights
Unknown Manufacturer
🏠 Consumer Products Class I - Dangerous
The lights lack adequate minimum wire size and overcurrent protection, posing fire and electrical shock hazards to consumers.
X-14® Mildew Stain Remover
Spartan Chemical Company Inc., of Maumee, Ohio
🏠 Consumer Products Class II - Moderate
Pressure can build up inside the bottle and cause it to fall over and leak, posing a risk of skin irritation.
Bio Source Naturals Wintergreen and Birch Sweet Essential Oils
Bio Source Naturals, of New Boston, Mich.
🏠 Consumer Products Class II - Moderate
The products contain the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products are not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
Valor H5 gas fireplace
Miles Industries Ltd., of Canada
🏠 Consumer Products Class I - Dangerous
Delayed ignition due to pilot degradation can cause gas in the fireplace to accumulate prior to burner ignition. When ignition takes place, it can cause the glass window to shatter, posing burn and laceration hazards.
Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM
Cj Haide (Ningbo) Biotech Co.
🍎 Food Class I - Dangerous
complaint of metal fragments
Undeclared walnut. Carrot Cake Layered Cheesecake was incorrectly decorated as Red Velvet Layered Cheesecake and was mis-labeled. Finished product label does not declare walnut.
💊 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.
💊 Drugs Class I - Dangerous
Superpotent Drug: Out-of-specification (OOS) result observed in an assay test of retention samples.
💊 Drugs Class I - Dangerous
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
💊 Drugs Class I - Dangerous
Chemical Contamination: Presence of Undeclared Methanol
💊 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.