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. 2,443 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,443 in last 12 months

Showing 1982119840 of 48,326 recalls

DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Facial Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Ithurts Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Immunexx Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Arthros Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Mesenchyme Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Infla Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-GI Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Prolo Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Neuro 3 Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-ANS/CNS Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Lymph 1 Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Collagen Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Intra-Cell Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Hair Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 14, 2019· Abbott Medical

Recalled Item: Radiofrequency Grounding Pad Recalled by Abbott Medical Due to Affected lots...

The Issue: Affected lots were manufactured with the protective release liner in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: 7% BSA (Bovine Serum Albumin) Recalled by Ortho Clinical Diagnostics Inc Due...

The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Becton Dickinson & Company

Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575...

The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Becton Dickinson & Company

Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547...

The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: Urine Electrolyte Diluent Recalled by Ortho Clinical Diagnostics Inc Due to...

The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Mizuho OSI

Recalled Item: Levo Arm Label: LEVO ARM MIZUHO OSI Recalled by Mizuho OSI Due to Due to the...

The Issue: Due to the potential for fluid ingress into the Arm which could affect the...

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

Class II — Potential Health HazardOngoing