State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 100 mg after the product failed dissolution specifications.
Olympus is recalling ShockPulse-SE Lithotripsy System reusable probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Aesculap is recalling MINOP Trocar 150 mm with 6.0 mm working channel, model FF399R, because of the potential for the trocar shaft to be too long.
Siemens Healthcare Diagnostics is recalling all lots of the Atellica CH Urine Albumin assay because falsely depressed patient results may occur above the measuring interval.
Olympus is recalling ShockPulse-SE Lithotripsy System single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Volkswagen is recalling certain 2025–2026 Jetta vehicles because the transmission ground wire may not have been properly connected during assembly, creating an open electrical circuit that could increase fire risk.
Volvo is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles because the seat belt warning system may not activate the audible warning chime. This fails FMVSS 208.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-210, because of the potential for rubber fragment detachment during use.
Mack Trucks is recalling 2022-2027 TerraPro trucks because engine software may allow starting while in gear, increasing crash risk.
ARBOC is recalling 2018-2026 Spirit of Freedom and Spirit of Mobility buses because incorrectly installed rear brake lines may cause the anti-lock brake system to malfunction.
Diagnostica Stago is recalling four lots of the STA Liatest Free Protein S kit because of the potential for out-of-range results and underestimation of free protein S in normal patient plasmas.
Acme United Corporation is recalling Med-Nap BZK Antiseptic Towelettes in bulk packs over current good manufacturing practice deviations.
Acme United Corporation is recalling Med-Nap Cleansing Towelettes in bulk cases over current good manufacturing practice deviations.
Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.
Acme United Corporation is recalling Max Packaging Antibacterial Towelettes over current good manufacturing practice deviations.
Acme United Corporation is recalling Dynarex BZK Antiseptic Towelettes in 1,000-packet bulk packs over current good manufacturing practice deviations.
The Harvard Drug Group is recalling one lot of Midodrine Hydrochloride Tablets 5 mg because of a defective container with inadequately sealed blister packaging.
Acme United Corporation is recalling Dynarex BZK Antiseptic Towelettes in 100-packet cartons over current good manufacturing practice deviations.
Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.
Acme United Corporation is recalling First Aid Only Hand Sanitizing Wipes over current good manufacturing practice deviations.
Acme United Corporation is recalling Med-Nap Cleansing Towelettes over current good manufacturing practice deviations.
HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 1 4% Lidocaine Cream because the stability data does not support the labeled expiry date.
Vascutek is recalling Gelsoft Plus and Gelweave vascular prostheses because they were labeled with an additional month of shelf life, expiry having been calculated from packaging rather than gel impregnation.
Datascope is recalling the CS100 IABP running software version Q.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.
HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 2 4% Lidocaine Cream because the stability data does not support the labeled expiry date.