State
73,381 recalls have nationwide distribution and so reach Oregon. 7,531 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,531 recalls naming Oregon we have scored against our rubric, 876 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,128 (28%) are Severe.
Which agencies issued them
These figures cover only the 7,531 recalls whose distribution notice names Oregon specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
S&B Filters is recalling certain diesel fuel tanks for RAM Mega Cab vehicles due to insufficient clearance that may cause fuel leaks and fire risk.
McKesson Medical-Surgical Inc. is recalling Triple Antibiotic Ointment due to storage deviations that violated drug label specifications and current good manufacturing practices.
Natierra Nature & Earth Organic Blueberries are recalled due to elevated lead levels detected by Maryland Department of Health testing. The recall affects 22,014 units distributed nationwide.
Cipla is recalling Difluprednate ophthalmic emulsion nationwide due to defective container closures that compromise sterility assurance. Patients using the affected lot should discontinue use and contact their healthcare provider.
PACCAR is recalling 2021 Peterbilt 220 and 2022 Kenworth K270 trucks because software may prevent stability control commands from processing during regenerative braking, increasing crash risk.
BatteryJack is recalling specific RS TN-0700 motorcycle helmets because they may not adequately protect the wearer in a crash, failing to meet federal safety standards.
HAIOU retractable safety syringes are recalled due to reports of needle detachment from the syringe after injection and failure to retract, increasing needle stick injury risk. Approximately 4.05 million units are affected.
Strides Pharma is recalling Prednisone 20 mg tablets due to contamination with 2.5 mg tablets. No illnesses have been reported, but patients may receive incorrect doses.
Mckesson Medical-Surgical has recalled Eye-stream eye wash solution nationwide due to storage conditions outside drug label specifications.
Roche is recalling approximately 965 cobas e801 Immunoassay Analyzers nationwide due to a software issue that impacts Pre-Wash test signals and results for six diagnostic assays. No injuries or illnesses have been reported.
SterRx is recalling FentaNYL Citrate intravenous bags (10 mcg/mL) due to lack of assurance of sterility. The recalled lot (CHI, expiring December 2022) was distributed nationwide.
GE Healthcare patient tables used in CT, PET, and NM systems can drop during service if technicians remove incorrect screws without appropriate supports, potentially injuring service personnel.
Genuine Scooters is recalling certain 2022 NIU MQiGT EVO scooters due to excessive handlebar vibration. The vibration may cause rider fatigue or loss of vehicle control, increasing crash risk.
ZADITOR eye drops were stored outside FDA label specifications in a nationwide Class II recall affecting 9 boxes distributed by McKesson Medical-Surgical Inc.
Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Vanilla Bean due to missing milk allergen declaration on the label. Consumers with milk allergies may be at risk.
Hikma Pharmaceuticals is recalling approximately 4.7 million vials of Lorazepam injection nationwide after finding out-of-specification related compounds during quality testing. The affected lots expire between June and August 2023.
SterRx is recalling 360 bags of fentanyl citrate IV medication due to lack of assurance of sterility. No illnesses have been reported.
Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Chocolate because the label declares whey but fails to declare milk. Approximately 2,747 bags were distributed nationwide.
A Corin MetaFix hip stem (size 7 collarless) was incorrectly labeled as a size 3 collared stem with wrong batch information. The labeling error creates risk during surgical implantation.
Hikma Pharmaceuticals is recalling Lorazepam Injection vials due to out-of-specification impurities and degradation products found during quality testing of retained samples.
Hikma Pharmaceuticals is recalling 82,700 vials of Lorazepam Injection due to failed quality specifications for impurities and degradation. Lot #070096 (expired July 2023) was distributed nationwide.
Mckesson Medical-Surgical is recalling ALCOHOL PREP sterile alcohol prep pads nationwide because they were stored outside manufacturer specifications, potentially compromising sterility. FDA classified this as a Class II recall.
PACCAR Incorporated is recalling certain 2023 Kenworth and Peterbilt commercial trucks because the engine control module may short-circuit, causing the engine to stall unexpectedly. An engine stall while driving increases the risk of a crash.
Smirks Ltd is recalling Organic Amaranth due to potential Salmonella contamination. The product was distributed across multiple states.
Xhibit Telemetry Receiver Model 96280 units fail to escalate critical alarms after approximately 25 days of continuous use, including signal loss, low battery, and SpO2 sensor issues. Caregivers may not be aware of device failures.