The Recall Desk

State

Montana product recalls

73,198 recalls have nationwide distribution and so reach Montana. 3,571 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,571
Critical
689
Severe
785
Most recent
2026-09-23

Of the 3,571 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 785 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,571 recalls whose distribution notice names Montana specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14851–14875 of 76769

  • HighFDA (Drugs)·D-1125-2023·2023-09-06

    FDA Recalls Phenylephrine IV Bags Due to Sterility Validation Concerns

    Central Admixture Pharmacy Services is recalling 586 bags of phenylephrine IV solution due to lack of validation data for sterilization cycles. These bags may not meet sterility assurance requirements for intravenous use.

    Product
    PHENYLephrine, added to 0.9% sodium chloride, 10mg/250ml (40mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6058-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1123-2023·2023-09-06

    Cardioplegia Solution Recalled Due to Lack of Sterility Assurance

    Central Admixture Pharmacy Services recalls Cardioplegia Solution due to lack of validation data for sanitization cycles, which cannot assure product sterility.

    Product
    CARDIOPLEGIA SOLUTION, 25 mEq K, SUTTER CARDIOPLEGIA, Total Volume = 572.64 mL, IV Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0217-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2491-2023·2023-09-06

    Olympus Bronchovideoscope Models Recalled Due to Lodging Risk in Connectors

    Olympus is recalling 1,072 units of Bronchovideoscope Models BF-MP160F, BF-XP160F, and BF-XP60 distributed nationwide. The devices can become lodged in the endotracheal tube connector due to oversized endoscope diameter.

    Product
    Olympus Bronchovideoscope, Models BF-MP160F, BF-XP160F, BF-XP60.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2485-2023·2023-09-06

    Philips Wireless Foot Switch for X-Ray Systems Risks Loss of Function During Procedures

    Philips is recalling wireless foot switches used with Allura Xper and Azurion X-ray systems because they may become unavailable during procedures. Approximately 1,865 units were distributed worldwide.

    Product
    Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2471-2023·2023-09-06

    Laboratory diagnostic test may produce inaccurate results from reagent carryover

    Siemens is recalling the Atellica CH Total Bilirubin diagnostic test because reagent carryover on the analyzer could produce falsely elevated results affecting multiple related lab tests.

    Product
    Atellica CH Total Bilirubin_2 -In vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma (lithium heparin) of adults and neonates Test Code: TBil_2 Siemens Material Number (SMN): 11097531
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2512-2023·2023-09-06

    Phoroptor VRx Digital Refraction System head detachment hazard recall

    Reichert's Phoroptor VRx Digital Refraction System head may detach from its mounting bracket and fall onto patients or operators. The recall affects 87 units distributed nationwide.

    Product
    PHOROPTOR VRX DIGITAL REFRACTION SYSTEM-Digital refractor intended for the subjective measurement of the refractive error of the eye. MODEL NUMBER: 16242 [Model 16241 is the base model. Model 16242 includes an additional prism feature used for the measurement of ocular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1132-2023·2023-09-06

    Sterile Injectable Drug Recall: oxyTOCIN in Lactated Ringer's IV Bags

    Central Admixture Pharmacy Services is recalling 1,996 bags of oxyTOCIN in Lactated Ringer's IV bags because the company cannot assure the products are sterile. The firm lacks validation data for its sanitization procedures.

    Product
    oxyTOCIN 30 units added to Lactated Ringer's 500 mL, IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6039-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2490-2023·2023-09-06

    Olympus Bronchovideoscope models recalled for lodging risk in airway connectors

    Olympus is recalling 1,715 Bronchovideoscope units across eight models due to a diameter defect that causes the device to lodge in the endotracheal tube connector.

    Product
    Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT160.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1142-2023·2023-09-06

    Sabril (vigabatrin) oral solution recalled for cross-contamination

    Lundbeck LLC recalls Sabril (vigabatrin) oral solution nationwide due to potential cross-contamination. The recall affects 10,543 cartons.

    Product
    SABRIL — SABRIL (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1269-2023·2023-09-06

    Siemens Atellica CH Total Protein II Recalled for Reagent Carryover

    Siemens Healthcare Diagnostics is recalling Atellica CH Total Protein II due to reagent carryover affecting magnesium test accuracy. The recall covers all lots (13,071 units) distributed nationwide and internationally.

    Product
    Atellica CH Total Protein II- In vitro diagnostic use in the quantitative determination of total protein in human serum and plasma (lithium heparin) using the Atellica CH Analyzer. SMN: 11097604
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1139-2023·2023-09-06

    Clindamycin Phosphate Topical Solution Recalled for Defective Container

    Contract Pharmaceuticals is recalling Clindamycin Phosphate Topical Solution USP 1% due to defective containers that leak under the cap. The recall affects 11,350 bottles distributed nationwide.

    Product
    Clindamycin Phosphate Topical Solution USP, 1%, 60 mL bottle, Rx only, Manufactured by: Contract Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, Manufactured for: Glasshouse Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, NDC# 71428-003-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V617000·2023-09-05

    Peterbilt and Kenworth trucks recalled for fuel hose production defects

    Remote Stage 2 fuel filter hoses in 2023-2024 Peterbilt and Kenworth trucks may be damaged, risking disconnection, engine stall, and fuel leaks that could cause fire or crashes.

    Product
    KENWORTH — KENWORTH, PETERBILT T280, T380, 536, 537
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V616000·2023-09-05

    PACCAR Recalls 2023 Kenworth and Peterbilt Trucks for Driveshaft Defect

    PACCAR is recalling 2023 Kenworth K270, K370, and Peterbilt 220 trucks because the driveshafts can break under certain loading conditions, increasing the risk of a crash.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, K370, 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V618000·2023-09-05

    Wilson Recalls One 2024 DWH-750 Trailer for Tire Pressure Loss

    Wilson Trailer Company is recalling one 2024 DWH-750 Pacesetter Grain trailer because the tire pressure regulation system may fail at speeds over 45 mph, increasing crash risk.

    Product
    WILSON — WILSON DWH-750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E066000·2023-09-05

    Covercraft Seat Covers Recalled for Incorrect Air Bag Deployment Risk

    Covercraft is recalling specific seat covers for Toyota, Ford, and Buick vehicles because incorrect thread may cause side-seat air bags to deploy incorrectly, increasing injury risk.

    Product
    SEATS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·040-2023·2023-09-02

    Banquet Frozen Chicken Strips Recalled for Plastic Contamination

    Conagra Brands is recalling Banquet Chicken Strips Meal due to possible plastic contamination that caused an oral injury.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — ConAgra Brands Inc. Recalls Banquet Brand Frozen Chicken Strips Entree Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V613000·2023-09-01

    Audi Recalls 2023 E-Tron GT Models for Battery Fire Risk

    Audi is recalling 2023 RS E-Tron GT and E-Tron GT vehicles because insufficient battery sealant may allow liquid accumulation, increasing the risk of electrical arcing and fire.

    Product
    AUDI — AUDI RS E-TRON GT, E TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V612000·2023-09-01

    2022 Silver Lake Travel Trailers Recalled for Detaching Sidewall Siding

    Forest River's 2022 Silver Lake and Della Terra travel trailers are being recalled because the aluminum sidewall siding may not be properly installed and could detach. Detached siding increases the risk of a crash or injury while towing.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V615000·2023-09-01

    2023 Porsche Taycan battery sealant defect increases fire risk

    Porsche is recalling 2023 Taycan vehicles with high-voltage batteries that may have insufficient sealant, allowing liquid accumulation that can cause electrical arcing and fire risk. Dealers will test and replace batteries free of charge.

    Product
    PORSCHE — PORSCHE TAYCAN TURBO S CROSS TURI, TAYCAN, TAYCAN CROSS TURISMO, TAYCAN TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23269·2023-08-31

    Frigidaire Gas Cooktops Recalled for Gas Leak and Fire Hazard

    Electrolux Group is recalling about 215 Frigidaire gas cooktops because plastic control knobs with black shafts can crack or break during use, creating a risk of gas leak and fire. Electrolux has received 63 reports of cracking or breaking, including one minor injury from a gas leak and one report of fire.

    Product
    Frigidaire Stainless-Steel 30-inch 4 Burner and 36-inch 5 Burner Gas Cooktops
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23788·2023-08-31

    Polaris MATRYX PRO RMK and MATRYX RMK KHAOS Snowmobiles Recalled for Puncture Hazard

    Polaris is recalling about 15,900 Model Year 2022–2023 MATRYX PRO RMK and MATRYX RMK KHAOS snowmobiles because handlebar hooks pose a puncture hazard and risk of serious injury during crashes. The firm has received four reports of puncture wounds.

    Product
    Polaris Snowmobiles, Model Year 2022-2023 MATRYX PRO RMK and MATRYX RMK KHAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V608000·2023-08-31

    Triple E Recalls 2021-2023 Unity Motorhomes Due to Fire Risk

    Triple E is recalling 2021-2023 Unity motorhomes because a battery disconnect switch may short circuit, increasing the risk of a fire.

    Product
    TRIPLE E — TRIPLE E UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide