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. 2,466 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,466 in last 12 months

Showing 1610116120 of 48,326 recalls

Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2MM CH 25G 4MM Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2MM CH 23G 6MM Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: B-V243Q-A 3-LUMEN EXTRACTION BALLOON V Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 5MM Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: CRESCENT SNARE Recalled by Aomori Olympus Co., Ltd. Due to Inspection...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-411D-1521 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: SD-210U-10 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 26G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX LOWER 23G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G Recalled by Aomori Olympus Co.,...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Ethicon, Inc.

Recalled Item: Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to...

The Issue: Product distributed with a red tape as part of the sterile packaging which...

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

Class II — Potential Health HazardOngoing
DrugJanuary 1, 2021· Precision Dose Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse USP 0.12% Recalled by Precision Dose Inc....

The Issue: cGMP deviations: The firm was notified of the manufacturer's expanded recall.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· AuroMedics Pharma LLC

Recalled Item: Acetaminophen Injection 1 Recalled by AuroMedics Pharma LLC Due to...

The Issue: Discoloration and failed pH specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· Allergan, PLC.

Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...

The Issue: Labeling: Missing instructions for use insert

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 30, 2020· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...

The Issue: The Quality Control (QC) card has a label error for the standard deviation...

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

Class II — Potential Health HazardOngoing
DrugDecember 28, 2020· Sunstar Americas, Inc.

Recalled Item: Paroex (Chlorhexidine Gluconate) Oral Rinse Recalled by Sunstar Americas,...

The Issue: cGMP Deviations; FDA inspection of manufacturing facility observed potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2020· Akorn, Inc.

Recalled Item: Levetiracetam Oral Solution Recalled by Akorn, Inc. Due to Defective...

The Issue: Defective container: Customer complaints for oral solution leaking from bottles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2020· New Standard Device Inc

Recalled Item: Metalogix Self-Drill Half-Pin Recalled by New Standard Device Inc Due to...

The Issue: Complaints were received for Self-drill Half-Pin tip breakages occurring...

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

Class II — Potential Health HazardOngoing