Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 6,651–6,700 of 15,271
- Class I
Medical Device Recall · May 14, 2025
Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS Software Version: N/A Product Description: The Edwards FEMFLEXII Arterial Perfusion Cannluae providesdue to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
- Class I
Medical Device Recall · May 14, 2025
Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae providesdue to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
- Class II
Drug Recall · May 14, 2025
AsttraZeneca Pharmaceuticals LP
Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation, packaged in a) 120-inhalation canister (NDC 0310-9080-12) b) 28-inhalation canister (NDC 0310-9080-28), Rx only, MDefective delivery system
- Class I
Medical Device Recall · May 14, 2025
Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterialdue to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
- Class I
Medical Device Recall · May 14, 2025
Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterialdue to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
- Class I
Medical Device Recall · May 14, 2025
Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae providesdue to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
- Class II
Medical Device Recall · May 13, 2025
Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD SmartFlow SKU 84021B Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow ControllerIncorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.
- Class II
Medical Device Recall · May 13, 2025
Product Name: SmartPath to dStream for 3.0T; Model Number: 782145Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: Upgrade to MR 7700; Model Number: 782130;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Food Recall · May 13, 2025
Nature Mills Traditional Rasam Powder, 200gUndeclared sesame and wheat allergens
- Class II
Medical Device Recall · May 13, 2025
Ami HTX.The X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.
- Class II
Drug Recall · May 13, 2025
Zydus Pharmaceuticals (USA) Inc
Esomeprazole Magnesium for Delayed-Release Oral Suspension, 40 mg, 30-count Single-Dose Packets per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus PhFailed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term stability.
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia 1.5T CX; Model Number: 781262;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
Drug Recall · May 13, 2025
Zydus Pharmaceuticals (USA) Inc
Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg, 30-count single dose packets per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus PhFailed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term stability.
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Food Recall · May 13, 2025
Nature Mills Traditional Sambar Powder, 200gUndeclared sesame and wheat allergens
- Class II
Drug Recall · May 13, 2025
Celecoxib Capsules, 200 mg, 50 Capsules (5x10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 50268-169-15Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
- Class I
Food Recall · May 13, 2025
AFGHANI CORN BREAD "Doda"; INGREDIENTS: Corn Flour, Sugar, Vegetable Oil, Eggs, Milk, Black Seeds, Caardamom; ALLERGEN STATEMENT: This product contains eggs, milk, and may contain traces of nuts. NETUndeclared allergens (wheat, sesame)
- Class II
- Class II
Food Recall · May 13, 2025
Kraft package is labeled as Hummingbird Organic Roasted Salted Cashews, net wt. 6oz.Undeclared hazelnut. The Oregon Trail Mix contains visible hazelnut and was mis-labeled as Organic Roasted Salted Cashews, but the label does not declare hazelnut.
- Class II
- Class II
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia 3.0T CX; Model Number: 781271;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
- Class II
- Class II
Medical Device Recall · May 13, 2025
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Medical Device Recall · May 13, 2025
SCD Comfort Knee Length Small, SKU 84021; Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow ControllerIncorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Medical Device Recall · May 13, 2025
Product Name: Ingenia 1.5T S; Model Number: 781347;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Medical Device Recall · May 13, 2025
Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- Class II
Medical Device Recall · May 13, 2025
Lago XThe X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.
- Class II
Medical Device Recall · May 13, 2025
Kendall SCD Comfort Sleeves Knee Length Small, Pediatric - For use with Kendall SCD SmartFlow, SKU 84021P Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow ControllerIncorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.
- Class II
Medical Device Recall · May 13, 2025
Allon 2001. Part Number: 200-00263An investigation into a report of the patient wrap (ThermoWrap), used with the Allon device, exceeding the set temperature determined that if: 1. The Human Sensor Board is disconnected from the Controller Board in the Allon device AND the temperature alarms are disabled, or 2. The Water In and Water Out and Thermostat sensors are disconnected from the Human Sensor Board AND the temperature alarms are disabled, the device will proceed to heat the water above the hardware fault limit without notifying the user of the faulty condition.