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. 2,548 recalls have been distributed to Montana in the last 12 months.
Showing 4861–4880 of 48,326 recalls
Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Software...
The Issue: Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold Hard Steel Plus Liquid Recalled by Supercore Products Group Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Steel Capsules packaged in 1 count blister packs in boxes of 10...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Umary Acido Hialuronico Recalled by SoloVital Due to Undeclared Diclofenac
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...
The Issue: Due to mislabeling of products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...
The Issue: Due to mislabeling of products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7100 Recalled by Datex-Ohmeda, Inc. Due to Potential issue that may...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 with Et Control. This anesthesia gas machine is Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 100. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance CS2 and Avance CS2 Pro. These anesthesia gas machines Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...
The Issue: There is a potential that the robotic system's instrument cart arm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...
The Issue: Incorrect GTIN number on carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.