State
73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Winter Water Factory is recalling about 46,500 infant jumpsuits, rompers, snap suits, dresses and bibs because snaps can detach and expose sharp prongs, posing choking and laceration hazards to young children.
Weldon Division of Akron Brass is recalling 860 electrical multiplex modules due to an extra resistor that can cause vehicle lighting to fail.
Thor Motor Coach is recalling certain 2022-2023 recreational vehicles due to cracked LP gas system fittings that may leak and increase fire risk. Dealers will replace the fittings free of charge.
About 300 BIBS Baby Glass Bottles sold nationwide are being recalled because hot liquids can cause the rubber bumper to shrink, making the bottle tilt and spill, posing a burn hazard.
Santa Cruz Bicycles is recalling about 1,600 of its 2022 Heckler 9 electric bicycles because the battery latch mechanism can malfunction, causing the battery to fall off the frame and posing a fall hazard to riders. The latch spring can also wear the battery housing over time, creating a fire hazard.
Suave 24-Hour Protection Aerosol Antiperspirant has been recalled nationwide due to the presence of benzene. The recall affects 4 oz. and 6 oz. cans bearing expiration date 9/30/2023.
Mylan Pharmaceuticals is recalling 89,665 vials of Insulin Glargine Injection (100 units/mL) due to missing labels on the vials. Affected patients should not use the product and should contact their healthcare provider.
Groundwork Coffee LLC recalled MIND-FULL Bar snacks distributed in California and Oregon because allergens were not properly declared on the product. The bars contain peanut butter and should not be consumed by those with nut allergies.
Intuitive Surgical recalled SureForm surgical staplers after tissue pushout events caused unexpected bleeding during procedures. The actual harm rate exceeded safety predictions.
The Puritan Bennett 980 Series Ventilator may fail to sound its audible alarm or display its visual alarm during critical alarm states, potentially delaying treatment response.
Celltrion USA Inc. is recalling Celltrion DiaTrust COVID-19 Ag Rapid Test kits distributed to facilities without valid CLIA certification. The tests were distributed nationwide from December 2021 through February 2022.
Olympia Pharmacy has recalled 45,935 vials of pharmaceutical diluent due to manufacturing compliance deviations. Environmental and personnel monitoring limits were exceeded and not properly investigated prior to October 2021.
Jayco is recalling 2020-2022 Precept motorhomes because the heat shield beneath the storage compartment may be too short, allowing exhaust heat to melt it and increase fire risk.
Olympia Compounding Pharmacy is recalling T-105 injectables nationwide due to manufacturing process deviations. Environmental and personnel monitoring failures prior to October 2021 were not properly investigated.
Siemens Healthcare is recalling IMMULITE 2000 hCG diagnostic systems due to potential sample carryover that could produce falsely elevated hCG test results.
Olympia Compounding Pharmacy is recalling NAD+ lyophilized powder (16,329 vials nationwide) due to failure to properly investigate environmental and personnel monitoring violations in manufacturing.
Olympia Compounding Pharmacy is recalling QM-4, a compounded injectable, for manufacturing control deviations. Environmental and personnel monitoring excursions were not properly investigated prior to October 2021.
Olympia Compounding Pharmacy is recalling 2005 vials of ST-2, a compounded pharmaceutical, nationwide due to manufacturing practice deviations and failures to properly investigate environmental and personnel monitoring excursions.
Olympia Compounding Pharmacy recalls 6,431 vials of Hydroxocobalamin B12 injection nationwide due to manufacturing quality control failures. Environmental and personnel monitoring systems prior to October 2021 did not properly investigate deviations from acceptable limits.
Kalmar is recalling 2015-2022 Ottawa T2 terminal tractors because the trailer parking brake may set unexpectedly, increasing crash risk.
Olympia Compounding Pharmacy recalls SB-6 injectable drug due to manufacturing deficiencies. Prior to October 2021, environmental and personnel monitoring procedures were not properly investigated.
Sight Sciences is recalling 921 TearCare version 1.0 SmartHubs ophthalmic devices distributed nationwide because they were distributed prior to FDA 510(k) clearance without premarket evaluation of their performance characteristics.
Olympia Compounding Pharmacy is recalling SB-4 due to manufacturing quality control failures. The company did not properly investigate environmental and personnel monitoring problems that occurred before October 2021.
Olympia Compounding Pharmacy recalls 1,679 vials of QM-3 injection medication nationwide due to failures in environmental and personnel monitoring during manufacturing.
Siemens syngo.via RT imaging software upgraded to VB60 automatically modifies laser configuration, potentially displaying incorrect laser offset coordinates during radiation therapy patient marking.