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. 2,359 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,359 in last 12 months

Showing 3074130760 of 48,326 recalls

Medical DeviceNovember 16, 2016· Medtronic Inc

Recalled Item: Affinity Fusion" Oxygenator with Integrated Arterial Filter Recalled by...

The Issue: Medtronic is initiating a voluntary product recall for specific lot numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2016· Roche Molecular Systems, Inc.

Recalled Item: LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is Recalled by...

The Issue: The LightCycler¿ 480 algorithm used for the LightMix¿ Zika rRT-PCR Test, EUA...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2016· Teleflex Medical

Recalled Item: Weck Facial Closure Systems have application in laparoscopic procedures for...

The Issue: The devices wings may become partially detached from the EFx Shield during use.

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

Class II — Potential Health HazardOngoing
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C All Natural Parmesan/Romano Grated Cheese Recalled by 4 C Foods, Corp....

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp....

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural Parmesan/Romano Grated Cheese Recalled by 4 C...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C All Natural 100% Imported Italian Pecorino Romano Cheese Recalled by 4 C...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: Cento Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: Cento Romano Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Encore Medical, Lp

Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...

The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2016· Akorn Inc

Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications; out-of specification value for homogeneity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2016· Ultimate Body Tox

Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund