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 4532145340 of 48,326 recalls

DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Errin (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Junel(TM) Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camila (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa(R) (levonorgestrel/ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Balziva(TM) (norethindrone and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2013· MCKESSON TECHNOLOGIES INC.

Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...

The Issue: There was an occurrence where the patient case data did not match the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Acist Medical Systems

Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...

The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· AGFA Corp.

Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...

The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...

The Issue: Non-Sterility; mold contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: All Compounded Products Recalled by Med Prep Consulting, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential for mold contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 14, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...

The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Synvasive Technology Inc

Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...

The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...

The Issue: Two unsealed pouches were found at an Edwards' distribution location in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Elekta, Inc.

Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...

The Issue: The Column rotation can accidentally be moved to a different position which...

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

Class II — Potential Health HazardOngoing