Home / Recalls
Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
December 10, 2025Medical DevicesFDA
Aizu Olympus Co., Ltd. recalls Olympus OER-Pro
Hazard: Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
December 10, 2025Medical DevicesFDA
Aizu Olympus Co., Ltd. recalls Olympus OER-Elite
Hazard: Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
December 10, 2025Medical DevicesFDA
Paragon 28, Inc. recalls Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S
Hazard: Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be able to mate properly with the associated mounting bolt. If nail (implant) cannot properly mate with instrumentation, the surgery potentially will need to be aborted.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX850. Product Number: 866470.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX800. Product Number: 865240.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX750. Product Number: 866471.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX700. Product Number: 865241.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX600. Product Number: 865242.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX550. Product Number: 866066.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX500. Product Number: 866064.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX450. Product Number: 866062.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX400. Product Number: 866060.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Patient Monitor MX100. Product Number: 867033.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Multi-Measurement Module X3. Product Number: 867030.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue Multi Measurement Server X2. Product Number: M3002A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP90. Product Number: M8010A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP80. Product Number: M8008A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP70. Product Number: M8007A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP60. Product Number: M8005A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP50. Product Number: M8004A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP40. Product Number: M8003A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP30. Product Number: M8002A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP20. Product Number: M8001A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP5. Product Number: M8105A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Philips North America Llc recalls IntelliVue MP2. Product Number: M8102A.
Hazard: Potential issue where the IntelliVue monitors did not alarm.
December 10, 2025Medical DevicesFDA
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.
Hazard: Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.
December 10, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn T
Hazard: Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls 8 in 1 STI Test Kit
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls 3 in 1 STI Test
Hazard: Distribution without premarket approval/clearance.
December 10, 2025Medical DevicesFDA
GET TESTED INTERNATIONAL AB recalls 2 in 1 Trichomonas / Gardnerella Test
Hazard: Distribution without premarket approval/clearance.