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. 2,359 recalls have been distributed to Montana in the last 12 months.
Showing 27641–27660 of 48,326 recalls
Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard 24-Hour Oral Care Kit q4 Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard 24-Hour Oral Care Kit q2 Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA...
The Issue: Instruments may, under certain specific circumstances listed below, fail to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit Recalled...
The Issue: Specific lots have been reported to produce falsely lower than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...
The Issue: The firm was marketing the Ondamed System in the US without marketing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...
The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corporation Due to Lack...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Customer complaints for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Argatroban Injection Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: D-ZINE Rapid Size and Strength capsules Recalled by HARDCORE FORMULATIONS...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA-STEN Rapid Size and Strength capsules Recalled by HARDCORE...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...
The Issue: A small number of batches may crack or break if exposed to certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.