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.

48,326 total recalls
2,359 in last 12 months

Showing 3080130820 of 48,326 recalls

Medical DeviceNovember 3, 2016· Olympus Corporation of the Americas

Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...

The Issue: Software malfunction that results in incorrect generation or display of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue where certain...

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2016· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: OOS results for known compound.

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Zydus...

The Issue: Failed Dissolution Specifications; 6 month time point

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens is releasing a software update that provides bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is releasing a software update that provides bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens is releasing a software update that provides bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile...

The Issue: Package may be incorrectly labeled as containing 0.76 mm Drill Bit, but in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the semi-automatic focus switch may not work as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the semi-automatic focus switch may not work as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the semi-automatic focus switch may not work as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· CareFusion 303, Inc.

Recalled Item: Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where...

The Issue: Reports where the Low Battery alarm and/or the Very Low Battery alarm are...

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

Class II — Potential Health HazardOngoing
DrugNovember 1, 2016· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Complaints of broken tips on the ampules.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg Recalled by Teva...

The Issue: Failed Content Uniformity: Product was out of specification for spray...

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg Recalled by Teva...

The Issue: Failed Content Uniformity: Product was out of specification for spray...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 31, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Flexible Shaft Recalled by Synthes (USA) Products LLC Due to...

The Issue: Non-conforming material used.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Sorin Group USA, Inc.

Recalled Item: Perceval Sutureless Aortic Heart Valve size S Recalled by Sorin Group USA,...

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the Perceval...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Spectranetics Corporation

Recalled Item: Turbo Elite Atherectomy Catheter. Models: 410-152 Recalled by Spectranetics...

The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche Recalled by Roche...

The Issue: Incorrect Urea results may be generated sporadically on cobas b 221<6>Roche...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Spectranetics Corporation

Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...

The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...

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

Class II — Potential Health HazardOngoing