State
73,584 recalls have nationwide distribution and so reach Oregon. 7,533 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,533 recalls naming Oregon we have scored against our rubric, 873 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,131 (28%) are Severe.
Which agencies issued them
These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker is recalling Hoffmann II Carbon Connecting Rods (catalog 50796040) because they may crack after cleaning and sterilization.
Medtronic is recalling its EOPA arterial cannula because pinhole leaks may occur during bypass, risking hypovolemia, vessel injury, and organ dysfunction.
Medtronic is recalling EOPA 3D Arterial Cannula 22FR because pinhole leaks may occur during cardiopulmonary bypass, potentially causing hypovolemia, vessel injury, hypotension, ischemia, and organ dysfunction.
Windstone Medical Packaging, Inc. is recalling specific lots of AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits because of potential unexpected variability in endotoxin levels.
Medtronic recalls 21,290 EOPA arterial cannulas (BLUNT 22FR) because pinhole leaks may occur during bypass, risking hypovolemia, vessel injury, hypotension, ischemia, and organ dysfunction.
Permobil is recalling M3 Corpus Power Wheelchairs with firmware version 1.26.2 because the firmware lacks a speed restriction when the seat lift exceeds 50 mm, which may cause falls or tip-overs.
Mellish Island Corp. is recalling 1,600 bottles of Super Skin dietary supplement because the label does not declare that its marine collagen comes from fish, a potential allergen.
Stryker is recalling Hoffmann II Carbon Connecting Rods (catalog 50796120) because the rods may crack after cleaning and sterilization. The recall covers 5,439 units distributed worldwide.
Instrumentation Laboratory is recalling the GEM Premier 5000 portable blood analyzer system because bar code reader wands may assign patient results to the wrong patient ID. The recall affects 21 units distributed nationwide.
Philips is recalling IQon Spectral CT systems because the clinical scan may not start automatically after Bolus Tracking, requiring manual triggering and potentially causing extra radiation exposure.
Stryker GmbH is recalling Stryker Hoffmann II Connecting Rod Micro 3 x 50mm due to a potential risk of the rods cracking after cleaning and sterilization.
Argon Medical Devices is recalling its L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm (REF 384620) because the hub may leak or crack, potentially causing therapy interruption, blood loss, or bloodstream infection.
Argon Medical Devices is recalling certain L-Cath PICC catheters because the hub may leak or crack, potentially causing blood loss, infection, or therapy interruption.
IsoTis OrthoBiologics, Inc. is recalling OsteoBallast and Ballast bone graft extenders because they may contain less demineralized bone matrix than intended.
Instrumentation Laboratory is recalling GEM Premier 5000 portable blood analyzer systems because BCR wands may assign patient results to an incorrect patient ID. FDA classifies this as Class II.
Instrumentation Laboratory is recalling the GEM Premier 5000 blood analyzer system because bar code reader wands may assign patient results to the wrong patient ID. The FDA has classified this as a Class II recall.
Micro Labs USA Inc. is recalling one lot of Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution nationwide because the container may have broken cap spikes and undeliverable drops.
Stryker is recalling Hoffmann II Connecting Rod Micro 3 x 30mm (catalog 50796030) because the rods may crack after cleaning and sterilization. FDA has classified this as Class II.
Mylan Pharmaceuticals is recalling one lot of Mycophenolate Mofetil for Injection, 500 mg/vial, because precipitate was found in the vials. The recall covers 5,688 vials distributed nationwide.
Philips is recalling 182 Ingenuity CT systems in the US because the clinical scan may not trigger automatically after Bolus Tracking, potentially causing patient rescan and extra radiation.
Rivian Automotive, LLC is recalling certain 2025-2026 R1S and R1T vehicles because the front turn signals may fail to illuminate or flash.
Stryker GmbH is recalling Stryker Hoffmann II Connecting Rod Micro 3 x 150mm due to the potential for the rods to crack following cleaning and sterilization processes.
Instrumentation Laboratory is recalling certain GEM Premier 5000 blood analyzer systems because the bar code reader wand may assign patient results to the wrong patient ID.
Permobil Inc. is recalling 715 M5 Corpus Power Wheelchairs (REF 120032) because firmware versions 1.27 through 1.57 lack drive inhibit logic, which may allow driving under restricted conditions and cause instability.
Philips is recalling certain CT scanners because the clinical scan may not start automatically after Bolus Tracking, which could require a patient rescan and expose them to additional radiation.