State
73,588 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.
Of the 3,572 recalls naming Montana we have scored against our rubric, 688 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 953 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,572 recalls whose distribution notice names Montana specifically. The 73,588 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newmar motorhomes equipped with Dometic 3-burner cooking stoves may have an overtightened saddle valve bolt that damages the seal, causing a gas leak and increasing fire risk. Owners should contact Newmar for a free remedy.
Thor Motor Coach is recalling certain 2021 Four Winds motorhomes with Dometic stoves due to a potential gas leak that could increase fire risk. The stove's saddle valve bolt may be overtightened, damaging the seal.
Polaris is recalling about 18,400 RZR recreational off-highway vehicles because the clutch can fail, posing an injury hazard. No injuries have been reported.
Starwest Botanicals is recalling organic elderberry because a customer test detected Salmonella. The product was distributed nationwide and to two Canadian customers.
Covidien is recalling Puritan Bennett 980 ventilators due to battery overheating and thermal damage risks that could cause burns or smoke exposure.
FCA US LLC is recalling 2020 Alfa Romeo Giulia vehicles because rear brake discs may fracture, potentially reducing braking performance and increasing crash risk.
H & H Remedies, LLC is voluntarily recalling 365 bottles of White Liniment due to Current Good Manufacturing Practice (CGMP) deviations.
Keystone is recalling 2019–2021 Outback recreational trailers for inadequate frame rail support that may cause buckling and crash risk. Owners should contact 1-866-425-4369 for the free frame reinforcement repair.
Lamborghini is recalling 2,831 2019-2020 Urus vehicles because high engine temperatures may damage the fuel line connector, causing a leak and increasing fire risk.
Stryker is recalling Zyphr Disposable Cranial Perforators because a crack in the inner bit could release metal fragments into the surgical site or cause delayed disengagement.
Baxter Healthcare is recalling specific lots of Bupivacaine Hydrochloride Injection due to the presence of black and transparent particles in the solution.
Fresenius Medical Care is recalling Liberty Select Cycler devices with software version 2.9.0 because a software error may cause the device to fail to recognize extra fluid, potentially leading to inadequate dialysis.
Shanghai United Imaging Healthcare is recalling five uCT 550 CT scanners because an incorrect delay timer display may expose operators to unnecessary radiation.
Shanghai United Imaging Healthcare Co., Ltd. is recalling four uCT 530 CT scanners because an incorrect delay timer may display, potentially exposing operators to unnecessary radiation.
Boston Scientific is recalling AMS 700 MS Pumps due to reports of difficulty activating the device to inflate cylinders.
Shanghai United Imaging Healthcare is recalling five uCT 760 CT scanners because a display error may cause operators to receive unnecessary radiation exposure.
Shanghai United Imaging Healthcare is recalling nine uMI 550 PET/CT systems because an incorrect CT scan delay timer may display, potentially exposing operators to unnecessary radiation.
Maquet Cardiovascular is recalling 51 Blood Monitoring Units (BMU 40) because the printed circuit boards do not meet IEC electrical safety standards for creepage distance.
Volkswagen is recalling certain 2021 Atlas and related models because the rear view camera may malfunction during startup, showing a black screen or frozen image, reducing visibility when reversing and increasing crash risk.
Starwest Botanicals is recalling specific lots of organic elderberry tea after a customer test detected Salmonella.
Teva Pharmaceuticals is recalling 133,829 bottles of Mesalamine Delayed-Release Tablets because stability testing revealed out-of-specification dissolution results.
AvKARE Inc. is recalling specific lots of Mesalamine Delayed-Release Tablets because they failed to meet dissolution specifications.
Aesthetics Biomedical is recalling 623 Vivace Electrosurgical Systems because a high-frequency output was not cleared for U.S. distribution.
H & H Remedies, LLC is voluntarily recalling 252 jars of Vapor Ointment due to Current Good Manufacturing Practice (CGMP) deviations.
H & H Remedies, LLC is voluntarily recalling 939 jars of Union (black) salve due to Current Good Manufacturing Practice (CGMP) deviations.