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. 2,277 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,277 in last 12 months

Showing 4526145280 of 48,326 recalls

DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: DMSO Aqueous Irrigation 50% Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Atropine Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Testosterone Cypionate/Testosterone Enanthate Injection Recalled by Pallimed...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Diazepam Injectable Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: MIC with B6 and B12 Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2013· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...

The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...

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

Class III — Low RiskOngoing
FoodMarch 25, 2013· Decoty Coffee Company, Inc

Recalled Item: Taco Seasoning Recalled by Decoty Coffee Company, Inc Due to Undeclared...

The Issue: Recently, DeCoty Taco Seasoning, 1.25 lb (Lot numbers 010111-021313) and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...

The Issue: Stryker Orthopaedics received a report that a label on the external...

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2013· Actavis Inc

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Watson Laboratories, Inc.-(Actavis) - Florida

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Actavis South Atlantic LLC

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg Recalled by...

The Issue: Failed USP Dissolution Test Requirements: Out-of-specification dissolution...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner & Reprocessor System Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) has determined that a limited number...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...

The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing