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 3504135060 of 48,326 recalls

Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 6F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 2F Recalled by...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Tracking Bracket Starter Kit Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Sales Demo Kit. Large Gauge Infiniti Plus Recalled by Civco Medical...

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 3F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Needle Guide Starter Kit Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2015· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION Recalled by Vintage...

The Issue: Failed Stability Specifications: Out of Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 21, 2015· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: Presence of Foreign Tablets/Capsules: one foreign capsule identified as...

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2015· Teva Pharmaceutical Industries

Recalled Item: Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg Recalled by...

The Issue: Labeling: Incorrect or Missing Lot AND/OR Exp Date.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart 10 Test Cup (PCP & MDMA) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 10-Panel Pipette Drug Screen Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: CLIA RDTC 12-Panel Cup and CLIA RDTC 12-Panel Cup (w/Adulteration) Recalled...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart 11 Test Cup Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: THERMO FISHER 6 DRUG CASSETTE Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 11 Panel Dip Card (OPI 2000) Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 12-Panel Dip Drug Screen with adulterant Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: Micro Screen 6 Panel Cup with Adult (AU) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: ArcPoint Labs 10 Panel Dip Screen (OXY) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing