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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
August 13, 2025Medical DevicesFDA
AVID Medical, Inc. recalls LAPAROSCOPIC TRAY. Medical convenience kit.
Hazard: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
August 13, 2025Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Pinnacle 3 with TumorLOC, (870258) Radiation Therapy Planning System Software
Hazard: Due to software issue, Radiation Therapy Planning system may provide incorrect dataset calculations when performing the "Stopping Power Ratio" (SPR) ,
August 13, 2025Medical DevicesFDA
Becton, Dickinson and Company, BD Bio Sciences recalls BD Trucount Controls, 30 Test - REF: 340335
Hazard: Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
August 13, 2025Medical DevicesFDA
Becton, Dickinson and Company, BD Bio Sciences recalls BD Trucount Controls, 30 Test - REF: 664343, RxOnly, IVD
Hazard: Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
August 13, 2025Medical DevicesFDA
Flexicare Medical (Dongguan) Ltd. recalls BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U
Hazard: Laryngoscope handles may not illuminate as intended.
August 13, 2025Medical DevicesFDA
Flexicare Medical (Dongguan) Ltd. recalls BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U
Hazard: Laryngoscope handles may not illuminate as intended.
August 13, 2025Medical DevicesFDA
Flexicare Medical (Dongguan) Ltd. recalls Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle REF:040-03-0000U
Hazard: Laryngoscope handles may not illuminate as intended.
August 13, 2025Medical DevicesFDA
Flexicare Medical (Dongguan) Ltd. recalls BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U
Hazard: Laryngoscope handles may not illuminate as intended.
August 13, 2025Medical DevicesFDA
Flexicare Medical (Dongguan) Ltd. recalls BritePro Solo Single-Use Fiber Optic Handle and Blade Refs: 040-331U (Mac 1), 040-332U (Mac 2), 040-333U (Mac 3),
Hazard: Laryngoscope handles may not illuminate as intended.
August 13, 2025Medical DevicesFDA
Flexicare Medical (Dongguan) Ltd. recalls BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref: 040-02-0110U (Mac 1), 040-02-0120U (Mac 2), 040-02
Hazard: Laryngoscope handles may not illuminate as intended.
August 13, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60
Hazard: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
August 13, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions
Hazard: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
August 13, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.
Hazard: Label is incorrect. The product label indicates that the device contains an air eliminating filter. However, the filter utilized on this extension set is not indicated for removal of air and does not feature an air vent, which is common to air eliminating filters.
August 13, 2025Medical DevicesFDA
ICU Medical, Inc. recalls Plum Duo Infusion System, List Number: 400020401
Hazard: ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.
August 13, 2025Food & BeverageFDA
Distinctive Foods LLC recalls Frederik's by Meijer Artisan Baked Sea Salt flatbread crackers net wt 5.5oz. UPC 7 13733 00048 2
Hazard: Undeclared sesame.
August 13, 2025Food & BeverageFDA
King Cheesecake Company, Inc. recalls Item #2485 Assorted layer cake
Hazard: Pecans have the potential to be contaminated with Salmonella
August 13, 2025Food & BeverageFDA
King Cheesecake Company, Inc. recalls Item #99273 chocolate Tres Leches Cheesecake
Hazard: Pecans have the potential to be contaminated with Salmonella
August 13, 2025Food & BeverageFDA
King Cheesecake Company, Inc. recalls Item #3145 Hummingbird Layer Cake
Hazard: Pecans have the potential to be contaminated with Salmonella
August 13, 2025Food & BeverageFDA
King Cheesecake Company, Inc. recalls Item #99272 Tres Leches Cheesecake
Hazard: Pecans have the potential to be contaminated with Salmonella
August 13, 2025Food & BeverageFDA
King Cheesecake Company, Inc. recalls Item #1312 Carrot layer cake
Hazard: Pecans have the potential to be contaminated with Salmonella
August 13, 2025Food & BeverageFDA
King Cheesecake Company, Inc. recalls Item #1071 Italian layer cake
Hazard: Pecans have the potential to be contaminated with Salmonella
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Yoplait Original Strawberry Banana Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003136
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Yoplait Original Harvest Peach Yogurt, 6 OZ (170g), packaged in a plastic cup, UPC: 170470003075
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Velveeta Slices Sharp Cheddar, 16 ct., NET WT 12 OZ (340g), packaged in plastic/cardboard, UPC: 021000044894
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Twister Fruit Punch, 59 FL OZ (1.84 QT) 1.75 L, packaged in a paper carton, UPC: 048500021231
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls 1) Simply Orange Pulp Free Orange Juice, 46 FL OZ (1.4 QT) 1.36 L, packaged in a plastic bottle, UPC: 025000136788 2) Si
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Silk Vanilla AlmondMilk, 64 FL OZ (2 QT) 1.89 L, packaged in a paper carton, UPC: 025293000995
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Shamrock Farms Whole Milk, 12 FL OZ (354 ML), packaged in a plastic bottle, UPC: 028300000896
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Shamrock Farms Chocolate Rockin' Protein Builder Protein Shake, 12 FL OZ (354 ML), packaged in a plastic bottle, UPC: 02
Hazard: Temperature abuse due to temperature excursion in one shipping trailer
August 13, 2025Food & BeverageFDA
Dollar General Corporation recalls Pillsbury Cinnamon Rolls Original Icing, 8 ct., NET WT 12.4 OZ (351g), packaged in a cardboard and aluminum tube, UPC: 0
Hazard: Temperature abuse due to temperature excursion in one shipping trailer