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. 2,410 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,410 in last 12 months

Showing 2004120060 of 48,326 recalls

Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Snap lock connectors provided within implantable port kits may not meet...

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

Class II — Potential Health HazardOngoing
DrugSeptember 18, 2019· Avella of Deer Valley, Inc. Store 38

Recalled Item: Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 18, 2019· GCP Laboratories Inc

Recalled Item: Major Infants' Gas Relief Drops Recalled by GCP Laboratories Inc Due to...

The Issue: Microbial Contamination of Non-Sterile Product.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2019· Akorn, Inc.

Recalled Item: Lidocaine Hydroclhoride Jelly USP Recalled by Akorn, Inc. Due to cGMP...

The Issue: cGMP Deviations: firm reported finding metal particulate matter in the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2019· Cook Inc.

Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...

The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· KT Health, LLC

Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...

The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· GE Healthcare, LLC

Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...

The Issue: Potential for failure of the patient leakage current test. There is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Icecure Medical Ltd

Recalled Item: IceCure Cryoablation System ProSense -Intended for cryogenic destruction of...

The Issue: Updated User Manual DSR3200000 Rev. E to include the safety guidelines in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2019· Draegar Medical Systems, Inc.

Recalled Item: The Infinity Acute Care System (IACS) Monitoring Solution with the Recalled...

The Issue: Cybersecurity vulnerabilities may cause device to reboot, lose alarm...

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

Class II — Potential Health HazardOngoing
FoodSeptember 13, 2019· Abbott Laboratories

Recalled Item: Abbott Calcilo XD Recalled by Abbott Laboratories Due to Off color and odor....

The Issue: Off color and odor. Compromised can seam due to product (powder) in the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2019· GUERBET LLC

Recalled Item: Optiray 320 (ioversol) Injection 68% Recalled by GUERBET LLC Due to...

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...

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

Class II — Potential Health HazardOngoing
Refund