State
72,913 recalls have nationwide distribution and so reach Montana. 3,567 additional recalls listed Montana specifically in their distribution scope.
Of the 3,567 recalls naming Montana we have scored against our rubric, 689 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 783 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,567 recalls whose distribution notice names Montana specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Merit Medical Systems, Inc. is recalling the Philips Bridge Prep Kit (Ref K12-09098C) because the catheter may experience resistance when being advanced over the guidewire during use.
Wells Pharma of Houston LLC is recalling 4,975 syringes of Ketamine Hydrochloride Injectable Solution (50 mg/mL) distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Philips is recalling the Ingenia 1.5T CX MRI machine with MR Elastography because certain image reconstruction parameters may cause stiffness value measurement errors in the default scan protocol.
Thea Pharma, Inc. is recalling iVIZIA Dry Eye (Povidone 0.5%) lubricant eye drops nationwide due to the FDA's discovery of manufacturing process deviations that affect the product's sterility assurance.
Philips is recalling specific units of SmartPath to dStream for XR and 3.0T with MR Elastography due to potential stiffness value errors when certain image reconstruction parameters are used with Resoundant's algorithm, which may cause voxel size settings in the default MRE scan protocol to display incorrectly.
Philips Ingenia 3.0T MRI systems with MR Elastography software may display incorrect stiffness values and voxel size settings when specific image reconstruction parameters are used, potentially affecting diagnostic accuracy.
Becton Dickinson is recalling certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems because gas generating sachets may produce carbon dioxide levels below specification.
Becton Dickinson & Co. is recalling certain lots of BD GasPak EZ Campy Gas Generating Pouch Systems because gas generating sachets may produce carbon dioxide levels below specification, potentially affecting microbiologic laboratory testing.
Philips Ingenia 1.5T MRI systems with MR Elastography may display incorrect stiffness values and voxel size settings due to image reconstruction parameter combinations. The error affects 54 units distributed worldwide.
DePuy Synthes is recalling 3 units of ATTUNE Revision Hinge Femoral RT SZ 8 CEM implants due to external sterile packaging adhered to internal sterile packaging, potentially compromising sterility.
American Regent, Inc. is recalling Levocarnitine Injection USP (1 g/5 mL) due to missing labeling on certain lots. The affected product was distributed nationwide.
CVS Lidocaine Wound Gel is being recalled because it failed pH specifications. The affected product is distributed nationwide.
Heraeus Medical is recalling PALAMIX duo dental mixing units (Material Number 66057897) because the mixing rod may come loose from its lock during use in units older than 1.5 years. The shelf life is being reduced from 3 years to 1.5 years.
Heraeus Medical is recalling PALAMIX uno dental material because the mixing rod may come loose during mixing in units older than 1.5 years. The shelf life has been reduced from 3 years to 1.5 years.
Winnebago is recalling 2026-2027 Solis recreational vehicles because the liquid propane hose may be routed over the exhaust heat shield, posing a fire risk.
Shyft Group is recalling 2025 Utilimaster Velocity vehicles because the cargo carrying capacity label may list an incorrect load value, potentially leading to overloading.
Gulf States Toyota, Inc. is recalling certain 2026 Toyota 4Runner vehicles because the load carrying capacity label is incorrect. This error may lead to improper vehicle loading and increase the risk of a crash.
Tesla is recalling certain vehicles running software version 2026.8.6 because the rearview camera image may be delayed when the vehicle is placed in reverse, breaching FMVSS 111.
Mercedes-Benz is recalling 2026 CLA 350 4MATIC and CLA 250+ EVs because the front passenger seat belt may remain locked, preventing proper restraint in a crash.
Braun Corporation is recalling 2026 Ram ProMaster vehicles because the rear bench seat may be missing two legs, which could fail to restrain occupants in a crash.
New Flyer is recalling 2022 XE40 transit buses because the speedometer may not illuminate when headlights are on, increasing crash risk.
Waymo is recalling 3,791 automated driving systems because software may allow vehicles to drive into standing water, increasing crash risk.
Mercedes-Benz USA is recalling 144,049 vehicles because the infotainment control unit may reset while the vehicle is in motion and cause the instrument panel display to go blank.
Thermos Stainless King food jars and Sportsman bottles are recalled after 27 reports of stoppers ejecting forcefully on opening, including three consumers with permanent vision loss.
Stephan Baby Boo Bunnie and Friends toys are recalled after 20 reports of the water-filled cube cracking or breaking, including one case where a child swallowed sharp pieces.