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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 4058140600 of 48,326 recalls

DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Welchol Tablets (colesevelam HCl) 625 mg Recalled by Daiichi Sankyo Pharma...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar HCT Tablets (olmesartan medoxomil Recalled by Daiichi Sankyo Pharma...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/25 mg...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide)...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar Tablets (olmesartan medoxomil) 20 mg Recalled by Daiichi Sankyo...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Benicar Tablets (olmesartan medoxomil) 40 mg Recalled by Daiichi Sankyo...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2014· Daiichi Sankyo Pharma Development

Recalled Item: Azor Tablets (amlodipine and olmesartan medoxomil) 10 mg*/40 mg Recalled by...

The Issue: Temperature Abuse; various products were not stored at Controlled Room...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container Recalled by...

The Issue: Presence of Particulate Matter: particulate matter identified as fibers...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 11, 2014· Baxter Healthcare Corp.

Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: particulate matter identified as fibers...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 11, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Presence of Particulate Matter: particulate matter identified as fibers...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 11, 2014· Jubilant Cadista Pharmaceuticals Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Jubilant...

The Issue: Presence of Foreign Substance: Tablets may contain dark blemishes identified...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2014· Sandoz Inc

Recalled Item: Orphenadrine Citrate Extended Release Tablets Recalled by Sandoz Inc Due to...

The Issue: Failed Dissolution Specifications: Product found to be out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 11, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Saturated Gauze Dressing Recalled by Amerx Health Care...

The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Daily Dressing Advanced 3-in-1 Hydrogel Recalled by Amerx Health...

The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management....

The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing...

The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing