Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,322 recalls have been distributed to Montana in the last 12 months.
Showing 40761–40780 of 48,326 recalls
Recalled Item: GreenSmoothieGirl TriOmega Superfood Recalled by Green Smoothie Girl Due to...
The Issue: The products contain Organic Sprouted Chia Powder that may be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...
The Issue: In certain circumstances, a software error can lead to a situation where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: When liquid comes in contact with the DX-D 100 touch screen, the device may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hospira MedNet Medication Management Suite (MMS). Product Usage: The...
The Issue: Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Canto and associated Fluidics Cart Product Usage: Flow Recalled by...
The Issue: Laser cooling fans and internal fan of the associated fluidics cart are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Qube Compact Monitor Recalled by Spacelabs Healthcare...
The Issue: Spacelabs Healthcare is recalling Qube Compact Monitor, Model 91390, due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets USP Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva is recalling one lot of Carbidopa...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kirkland Signature Coarse Ground Malabar Pepper Recalled by Olde Thompson,...
The Issue: Olde Thompson is recalling Kirkland Signature Coarse Ground Malabar Black...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DMI Duro-Med Industries Rollator Transport Chair Recalled by Briggs Medical...
The Issue: There have been 5 customer reports of a 501-1018 series DMI Rollator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee and Artis zeego systems. x-ray Recalled by Siemens Medical...
The Issue: There is a potential problem with Artis zee and Artis zeego systems running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...
The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.