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. 2,306 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,306 in last 12 months

Showing 4220142220 of 48,326 recalls

FoodDecember 17, 2013· International Foodsource, LLC

Recalled Item: Valued Naturals Natural Coconut Net wt. 8oz (216.80g) Imported by Recalled...

The Issue: NYSDAM Laboratory Analysis Reports has determined that Valued Naturals...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 17, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine...

The Issue: Bicarbonate Jug Adapter distributed prior to 510(k) approval

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens ADVIA 1200 and ADVIA 1650 Chemistry Systems. Automated Recalled by...

The Issue: An overflow flag //// is displayed in the result column for a test when the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 2MM Carbide Fluted Ball Recalled by The...

The Issue: Some carbide cutting burr fractured during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Recalled by...

The Issue: Some carbide cutting burr fractured during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part #...

The Issue: Some carbide cutting burr fractured during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 2MM Carbide Fluted Ball Recalled by...

The Issue: Some carbide cutting burr fractured during use.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 16, 2013· Bracco Diagnostics Inc

Recalled Item: VoLumen Barium Sulfate Suspension (0.1 % w/v Recalled by Bracco Diagnostics...

The Issue: Failed Stability Testing: This product is below specification for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2013· Qualitest Pharmaceuticals

Recalled Item: Cetirizine Hydrochloride Syrup (Cetirizine Hydrochloride Oral Solution...

The Issue: Failed impurities/degradation specifications; out of specification for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee Ceiling Systems. Angiographic x-ray system. Recalled by...

The Issue: During the lifetime of Artis zee Ceiling systems, there is an increased wear...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100S Sterilization System Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Covidien

Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...

The Issue: Covidien is conducting a voluntary field corrective action on Puritan...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugDecember 13, 2013· Corepharma LLC

Recalled Item: Pyridostigmine Bromide Tablets USP Recalled by Corepharma LLC Due to Failed...

The Issue: Failed Dissolution Specification: Corepharma Inc. is recalling...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...

The Issue: Ensuring all customers have the tools to assist in verifying the setting of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 12, 2013· Hospira Inc.

Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 12, 2013· Bee International, Inc.

Recalled Item: Candy Sweet Spots Recalled by Bee International, Inc. Due to Undeclared Egg

The Issue: Bee International is recalling Sweet Spots Candy because it has undeclared...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 12, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: Sterility of medical devices intended for use in surgical procedures may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing