State

Montana product recalls

73,584 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total: 3,572
Critical: 688
Severe: 953
Most recent: 2026-10-14

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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27626–27650 of 77156

HighFDA (Devices)·Z-0565-2021·2020-12-23
Terumo Capiox FX25 Advance Oxygenator Recall for Configuration Error
Terumo is recalling Capiox FX25 Advance Oxygenators because they may have the incorrect East or West configuration. The recall affects 5,079 units distributed in the US and abroad.
Product
(1) Capiox FX25 (West) Advance Oxygenator- with left port, 4-liter Reservoir, XC modified to Advance, Sterile Catalog Number: 3CX*FX25RWC (2) Capiox FX25 (East) Advance Oxygenator - FX25 with right port, 4-liter Reservoir, XC modified to Advance Catalog Number…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0152-2021·2020-12-23
Taro Recalls HEB Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling HEB Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
HEB — HEB (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0634-2021·2020-12-23
Roche Recalls Tina-quant C-Reactive Protein Gen.3 Reagents Due to Cross-Contamination
Roche is recalling Tina-quant C-Reactive Protein Gen.3 reagents due to cross-contamination causing invalid calibrations and low quality control recovery.
Product
Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative determination of CRP in human serum and plasma on Roche automated clinical chemistry analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0157-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling Best Choice Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Best Choice, Clotrimazole Cream, USP 1%, Antifungal, NET WT 0.5 OZ (14.2g), Distributed by: Valu Merchandisers, CO . 5000 Kansas Ave. Kansas City, KS 66106 Made in Canada. UPC 0-70038-20355-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0167-2021·2020-12-23
AvKARE Recalls Sildenafil Tablets Due to Packaging Mix-Up with Trazodone
AvKARE Inc. is recalling 38,715 bottles of Sildenafil 100 mg tablets because they were inadvertently packaged with trazodone at a third-party facility.
Product
Sildenafil Tablets USP 100 mg, Rx Only, 100-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-748-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0156-2021·2020-12-23
Taro Recalls Rite Aid Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Rite Aid Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
RiteAid Pharmacy RIngworm Cream, Clotrimazole Cream USP, 1%, Antifungal NET W 0.5 oz. (14.2g), Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011 Made in Canada. UPC 0 11822 53812 1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0155-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0635-2021·2020-12-23
Helena Laboratories Recalls K-ACT Actalyke Clotting Test Tubes
Helena Laboratories is recalling K-ACT Actalyke Clotting Test Tubes due to complaints of cracked or split caps.
Product
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0169-2021·2020-12-23
Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures
Hikma Pharmaceuticals is recalling 1.3 million vials of Sodium Chloride Injection USP 0.9% because pH test results were out of specification.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2021·2020-12-23
Medline Recalls RevMedX Trauma Dressings Due to Package Seal Integrity Issues
Medline Industries is recalling RevMedX Trauma Dressings because of package seal integrity issues. The recall affects 15,780 units distributed in the US and several international countries.
Product
RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per Case; Sterile - Product Usage: are intended to absorb exudates.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0612-2021·2020-12-23
Medtronic Percept PC Neurostimulator Recall Due to Software Connection Failure
Medtronic is recalling 12 Percept PC Implantable Neurostimulators because a software anomaly in the A620 Patient Programmer prevents connection to the device.
Product
Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0180-2021·2020-12-23
Fusion Health Recalls Pharmorigins Core Supplement for Unapproved Additive
Fusion Health and Vitality LLC is recalling Pharmorigins Core dietary supplements due to the unapproved use of a food additive and unapproved marketing statements.
Product
PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0159-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling specific lots of Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal Cream, NET WT 1 oz (30 g), Distributed by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10531. Made in Canada. UPC 3 51672 20022 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0570-2021·2020-12-23
Zimmer Biomet Recalls Polaris Spinal System Screws for Labeling Update
Zimmer Biomet is updating instructions for Polaris and Cypher spinal screws to warn against using them with direct current stimulation due to construct failure risks.
Product
Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0158-2021·2020-12-23
Taro Recalls TopCare Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling TopCare Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
TOPCARE — TOPCARE (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0154-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Athlete's Foot Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0146-2021·2020-12-23
Zydus Recalls Lansoprazole Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling 22,848 cartons of Lansoprazole 30 mg tablets nationwide because they failed to meet dissolution specifications.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0151-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Impurity
Taro Pharmaceuticals is recalling Equate Athlete's Foot cream because an unknown impurity was detected above specification limits.
Product
CLOTRIMAZOLE — CLOTRIMAZOLE (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0148-2021·2020-12-23
Biogen Recalls Vumerity Capsules Due to Dissolution Test Failures
Biogen is recalling 5,307 bottles of Vumerity capsules because they failed dissolution testing. The medication may not release the drug as intended.
Product
VUMERITY — VUMERITY (DIROXIMEL FUMARATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0153-2021·2020-12-23
Taro Recalls Kaiser Permanente Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling specific lots of Kaiser Permanente Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Kaiser Permanente Clotrimazole Cream USP, 1% Antifungal Cream, NET WT 1 oz (28.4 g), Manufactured by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T1C1 Distributed by Kaiser Foundation Hospitals Livemore, CA 94551-9756. Made in Canada. NDC 0179-8014-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V808000·2020-12-22
GM Recalls 2020 Chevrolet Bolt EV for Brake Caliper Fracture Risk
General Motors is recalling 2020 Chevrolet Bolt EV vehicles because a front left brake caliper may fracture, potentially reducing brake performance and increasing crash risk.
Product
CHEVROLET — CHEVROLET BOLT EV
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V809000·2020-12-22
Escape Trailer Recalls 2020 RVs Due to Gas Leak Risk
Escape Trailer is recalling 2020 RV trailers because a stove component may cause a gas leak, increasing the risk of fire.
Product
ESCAPE — ESCAPE ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21715·2020-12-22
2021 Can-Am Outlander and Renegade ATVs Recalled for Rear Wheel Separation
Bombardier Recreational Products is recalling 2021 Can-Am Outlander and Renegade ATVs because a rear wheel can separate, causing a crash hazard.
Product
2021 Can-Am Outlander and Renegade All-Terrain Vehicles (ATVs)
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·20V764000·2020-12-21
GM Recalls 2010-2013 Buick and Chevrolet Models for Rear Suspension Defect
General Motors is recalling specific Buick and Chevrolet vehicles because excessive corrosion protection on rear toe links may cause them to fracture, increasing crash risk.
Product
BUICK — BUICK, CHEVROLET LACROSSE, REGAL, MALIBU
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V802000·2020-12-21
Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Brake Fluid Leak
Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because rear brake calipers may leak fluid, allowing air into the hydraulic brake system.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
Category
Vehicle
Distribution
Distributed nationwide