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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
July 2, 2025Medical DevicesFDA
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 382633, BD Insyte Autoguard BC Winged, Shielded IV Catheter with Blood Control Technology, 20GA x 1.00 in (1.1x25 m
Hazard: Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
July 2, 2025Medical DevicesFDA
Becton Dickinson Infusion Therapy Systems, Inc. recalls REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
Hazard: Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
July 2, 2025Medical DevicesFDA
Jolife AB recalls LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult
Hazard: Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.
July 2, 2025Medical DevicesFDA
BIGFOOT BIOMEDICAL recalls Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release Configuratio
Hazard: Due to a software/firmware issue diabetes management system may provide a device error and cause the insulin pen to become unresponsive and unable to function. This error may pose a potential health risk for people living with diabetes as they may not have all information necessary to make a timely treatment decision.
July 2, 2025Medical DevicesFDA
Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer C11137
Hazard: Analyzer has calibration issues where curves switched from passed to failed due to system errors during aspiration. This anomaly causes erroneous results and delays if unnoticed. RLU values may be misinterpreted as valid measurements by LIS.
July 2, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
Hazard: There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.
July 2, 2025Medical DevicesFDA
Barco N.V. recalls Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300
Hazard: Cathode ray tube display system encoders and decoders have same MAC address; new system setup with two or more affected units can lead to systems not functioning reliably:audio, video and/or control signals might be interrupted or fall away, displays might switch to failover and back multiple times, devices/sources/sinks might not be discovered/available, might lead to delayed/prolonged procedures
July 2, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow So
Hazard: Lack of sterility assurance.
July 2, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls Extended Tip Applicator 8CM, Box of 1.
Hazard: Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.
July 2, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls Extended Tip Applicator, 15 CM, Box of 5.
Hazard: Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.
July 2, 2025Medical DevicesFDA
Integra LifeSciences Corp. (NeuroSciences) recalls Extended Tip Applicator, 8CM, Box of 5.
Hazard: Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.
July 2, 2025Medical DevicesFDA
SunMed Holdings, LLC recalls Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36
Hazard: The impacted tape was manufactured with incorrect information on the tape. Incorrect values are printed in the Red zone, Orange zone, and Grey zone. Using the incorrect values in the Red zone could lead to shocking a patient with an excessive dose of joules, causing significant harm including burns, heart damage, and cardiac arrest. Incorrect values in the Orange zone could lead to overdosing the patient with sodium bicarbonate and cause metabolic alkalosis, electrolyte imbalances, tissue damage, and worsen respiratory status. Incorrect information in the Grey may lead to underdosing the patient with sodium bicarbonate and may cause reduced myocardial contractility, decreased response to vasopressors, and increased risk of dysrhythmia.
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Spicy Shrimp Poke Bowl
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Duo Crispy Veg Shrimp 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Duo Crunchy Veg Shrimp 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Duo Crispy Calif Shrimp 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Duo Crunchy Calif Shrimp 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Duo Spicy Veg Shrimp 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Duo Spicy Calif Shrimp 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Rock N Roll Shrimp 10Ct
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Red Dragon Roll
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Crunchy Shrimp Roll
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Hy-Vee recalls Crispy Shrimp Roll 10Pc
Hazard: Potential contamination with Listeria monocytogenes
July 2, 2025Food & BeverageFDA
Isabelle's Kitchen, Inc. recalls Isabelle's Kitchen, Inc, Maple Avenue Foods Crunchy Wheatberry Salad , 5 lb., High density polyethylene container with s
Hazard: Product has Salmonella contamination
July 2, 2025Food & BeverageFDA
Isabelle's Kitchen, Inc. recalls Isabelle's Kitchen, Inc, Maple Avenue Foods Mediterranean Pasta Salad , 4.5 lb., High density polyethylene container wit
Hazard: Product has Salmonella contamination
July 2, 2025Food & BeverageFDA
Isabelle's Kitchen, Inc. recalls Isabelle's Kitchen, Inc, Maple Avenue Foods Quinoa Tabouli Salad , 5 lb., High density polyethylene container with seal
Hazard: Product has Salmonella contamination
July 2, 2025Food & BeverageFDA
Isabelle's Kitchen, Inc. recalls Maple Avenue Foods Powerhouse Wheatberry Salad Kit, 4.5lbs, High density polyethylene container with sealed lid
Hazard: Product has Salmonella contamination
July 2, 2025Food & BeverageFDA
Isabelle's Kitchen, Inc. recalls Isabelle's Kitchen, Inc, Greek Pasta Salad, 4.5 lb., High density polyethylene container with sealed lid. Kings Where I
Hazard: Product has Salmonella contamination
July 2, 2025Food & BeverageFDA
Preventics, Inc. dba Legere Pharmaceuticals recalls Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Pr
Hazard: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
July 2, 2025Food & BeverageFDA
Preventics, Inc. dba Legere Pharmaceuticals recalls NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a U
Hazard: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.