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.

27776–27800 of 77156

HighFDA (Devices)·Z-0513-2021·2020-12-09
Biomeme SARS-CoV-2 PCR Test Recalled for False Positive Results
Biomeme is recalling 105 units of its SARS-CoV-2 Real-Time RT-PCR Test because the software made false positive calls due to assay issues.
Product
The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in vitro diagnostic test that is based on widely used nucleic acid amplification technology. The Biomeme SARS-CoV-2 Real-Time RT-PCR Test contains primers and probes and internal controls used in RT-PCR for the in vitro…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21047·2020-12-09
CRAFTSMAN 10-Inch Corded Chain Saws Recalled for Laceration Hazard
Black & Decker is recalling CRAFTSMAN 10-inch corded chain saws with extension poles because they may start unexpectedly, posing a laceration risk.
Product
CRAFTSMAN® CMECSP610 10-inch corded chain saws with extension poles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0506-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Infection Risk Mitigation
Olympus is recalling ultrasound endoscopes to reduce the risk of patient infections by adding a new inspection step to the cleaning and disinfection instructions.
Product
Olympus Ultrasound Endoscope, Model number: GF-UCT160-OL5 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21042·2020-12-09
Neptune Benson Recalls Delta UV Generators for Pools Due to Fire Hazard
Neptune Benson is recalling Delta UV EA-4H-10 generators for pools and spas because water leaks can cause overheating and fire. No injuries have been reported.
Product
Delta UV EA-4H-10 ultra-violet generators installed in swimming pools and swim spas
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0507-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Infection Risk Reduction
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UE160-AL5 - Product Usage: used for endoscopic ultrasonic imaging of the gastrointestinal wall, bile and pancreatic ducts and surrounding organs.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21050·2020-12-09
Goal Zero Recalls Yeti 25A Fast Charge Power Supplies Due to Fire Hazard
Goal Zero is recalling approximately 4,500 Yeti 25A Fast Charge power supplies because loose connections can overheat and cause a fire. No injuries have been reported.
Product
Yeti 25A Fast Charge Power Supplies
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0520-2021·2020-12-09
K2M Recalls Yukon Anti-Torque Alignment Tubes Due to Manufacturing Defect
K2M, Inc. is recalling four Yukon Anti-Torque Alignment Tubes from Lot KTGG because shafts do not pass through the inner cannula, potentially delaying surgery.
Product
Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment Tube (the Alignment Tube ) provides counter rotation to reduce the torque applied to the anatomy when the size 15 Torque limiting shaft (the shaft is used to tighten the Yukon…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0499-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model Number: GF-UCT140-AL5 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0503-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UMQ130 - Product Usage: used with an Olympus Endoscopic Ultrasound Center, EVIS Video System Center, light source, documentation equipment, video monitor, Endo-Therapy accessories and other ancillary equipment for endoscopic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0500-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UCT180 - Product Usage: used with an Olympus universal endoscopic ultrasound center or a diagnostic system (ALOKA CO. LTD), video system center, light source, documentation equipment, monitor, EndoTherapy accessories and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0528-2021·2020-12-09
CME America Recalls Neofeed Syringe Pumps Due to Motor Wear and Cracks
CME America is recalling 4,182 Neofeed syringe pumps because motor wear may cause under-infusion without alarms and cracks may allow cleaning fluids to damage hardware.
Product
CME America T-Syringe Pump - Neofeed - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21043·2020-12-09
Spirit Halloween Recalls Children's Flashlights Due to Fire and Burn Hazards
Spirit Halloween is recalling about 6,100 children's flashlights because the batteries can overheat, posing fire and burn hazards.
Product
Children's flashlights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0498-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Infection Risk Mitigation
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UCT140P-AL5 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21048·2020-12-09
Washington Shoe Company Recalls Western Chief Toddler Rain Boots Due to Choking Hazard
Washington Shoe Company is recalling Western Chief toddler light-up rain boots because rivets on the handles can detach, posing a choking hazard to children.
Product
Western Chief toddler light-up rain boots
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2021·2020-12-09
Canon Flat Panel Monitor Recall Due to Cable Breakage Risk
Canon Medical System is recalling 14 CAS-930A Flat Panel Monitors because the cable may break during procedures, potentially causing delays or vessel damage.
Product
CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers: Infinix-8000C and Infinix-8000H - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V761000·2020-12-09
2021 BMW vehicles recalled for defective 48-Volt battery connections
BMW is recalling certain 2021 model vehicles due to improper assembly of the 48-Volt battery and starter-generator connection, which can increase electrical resistance and fire risk. Dealers will inspect and replace the connection if necessary.
Product
BMW — BMW X5, 530I, X6, X7
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21049·2020-12-09
GrillBlazer Recalls Propane Torch Guns Due to Fire Hazard
GrillBlazer is recalling Su-VGun and GrillGun propane torch guns because propane gas can leak, posing a fire hazard. No injuries have been reported.
Product
Su-VGun and GrillGun propane torch guns
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·21045·2020-12-09
Burley Recalls Dash X FM Child Bicycle Seats Due to Crash Hazard
Burley is recalling Dash X FM child bicycle seats because the reclining plate can detach, making the seat unstable and causing a crash hazard.
Product
Dash® X FM child bicycle seats
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2021·2020-12-09
CME America T-Syringe Pump T34 Recalled for Motor Wear and Hardware Cracks
CME America is recalling 4,182 T-Syringe Pump T34 units because motor wear may cause silent under-infusion and cleaning fluids may crack hardware.
Product
CME America T-Syringe Pump - T34 - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20E090000·2020-12-09
Ford F-250 and F-350 pickup trucks recalled for potential steering lock-up
Icon Vehicle Dynamics is recalling Ford F-250 and F-350 pickup trucks sold with its centerline stabilizer kit. The foam ring in the shock assembly may block piston ports, causing steering to lock up and increasing crash risk.
Product
FORD — FORD F-350 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0504-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Infection Risk
Olympus is recalling ultrasound endoscopes to reduce the risk of patient infections by adding a new inspection step to the cleaning instructions.
Product
Olympus Ultrasound Endoscope, Model number: GF-UM160 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0515-2021·2020-12-09
Capnostream 35 Portable Respiratory Monitor Recalled for False Temperature Display
Covidien LLC is recalling 3,217 Capnostream 35 Portable Respiratory Monitors because they may display a false 'Temperature Exceeds Limits' message and shut down without an alarm.
Product
Capnostream 35 Portable Respiratory Monitor, Product numbers PM35MN02, PM35MN01, PM35MN05, DLPM35MN02 - Product Usage: use during both no motion and motion conditions and for patients who are well or poorly perfused.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0112-2021·2020-12-09
Golden State Medical Supply Recalls Aripiprazole Tablets for Dissolution Concerns
Golden State Medical Supply is recalling Aripiprazole 15 mg tablets due to potential out-of-specification dissolution limits.
Product
ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS, Incorporated, Camarillo, CA 93012 USA, NDC #60429-449-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0511-2021·2020-12-09
ICU Medical Recalls IV Administration Sets with Incorrect Filter Assemblies
ICU Medical is recalling 1,100 units of smallbore IV administration sets due to incorrect filter assemblies. The products were distributed nationwide.
Product
REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron Filter, 3 Clamps (Blue, Yellow, White), Rotating Luer - Product Usage: The intravascular administration set is a single use, sterile, non-pyrogenic device, which…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0522-2021·2020-12-09
Chromsystems Recalls MassChrom Cortisol Saliva Control Level I Vials
Chromsystems is recalling 880 vials of MassChrom Cortisol, Cortisone Saliva Control Level I because the control lots may not meet stability criteria, potentially causing increased patient results.
Product
MassChrom Cortisol, Cortisone Saliva Control Level I, Order No. 0349 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide