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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 1, 2026Medical DevicesFDA
Philips Ultrasound, Inc recalls Philips OMNI II TEE Ultrasound Transducer
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
April 1, 2026Medical DevicesFDA
Philips Ultrasound, Inc recalls Philips Mini Multi TEE Ultrasound Transducer
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
April 1, 2026Medical DevicesFDA
Philips Ultrasound, Inc recalls Philips L17-5 Ultrasound Transducer
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
April 1, 2026Medical DevicesFDA
Philips Ultrasound, Inc recalls Philips L12-5 Ultrasound Transducer
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
April 1, 2026Medical DevicesFDA
Philips Ultrasound, Inc recalls Philips C9-4 Ultrasound Transducer
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
April 1, 2026Medical DevicesFDA
Philips Ultrasound, Inc recalls Philips 3D6-2 Ultrasound Transducer
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
April 1, 2026Medical DevicesFDA
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Hazard: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
April 1, 2026Medical DevicesFDA
Philips Respironics, Inc. recalls Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
Hazard: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
April 1, 2026Medical DevicesFDA
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Hazard: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
April 1, 2026Medical DevicesFDA
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
Hazard: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
April 1, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
Hazard: The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
April 1, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.
Hazard: The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
April 1, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
Hazard: The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
April 1, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
Hazard: The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
April 1, 2026Medical DevicesFDA
Beckman Coulter, Inc. recalls MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining ant
Hazard: Due to the likely presence of contamination in well(s).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls Brand Name: I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix) with the below descriptions and corresponding art
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers. 1. Cortical Screw; A
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated; Article Numbers: 31207-10, 31207-12, 31
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with the below descriptions and corresponding
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and correspo
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corresponding article numbers. 1. DFL (Di
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers. 1. Corti
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers. 1.
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw;
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls I.T.S. Screw System with the below descriptions and corresponding article numbers. 1. Cancellous Screw, Cannulated;
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article numbers. 1. Forea
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls Olecranonplate with Angular Stability with the below descriptions and corresponding article numbers. 1. Olecranon Hoo
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral T
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
April 1, 2026Medical DevicesFDA
I.T.S. GmbH recalls Brand Name: Humeral Head Plate with Angular Stability, with the following description: Proximal Humeral Plate. Article N
Hazard: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).