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. 2,340 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,340 in last 12 months

Showing 3578135800 of 48,326 recalls

DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Mupirocin Calcium Cream Recalled by GlaxoSmithKline, LLC. Due to Penicillin...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban (mupirocin calcium) Nasal Ointment Recalled by GlaxoSmithKline,...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 11, 2015· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...

The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: The Centricity...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· Synthes (USA) Products LLC

Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...

The Issue: DLS pin breakage during planned implant removal, after uneventful and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Cadiere Forceps Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Medium -Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Fenestrated Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing