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. 2,461 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,461 in last 12 months

Showing 1790117920 of 48,326 recalls

Medical DeviceJune 8, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...

The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...

The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2020· Hocoma AG

Recalled Item: Lokomat Pro Recalled by Hocoma AG Due to The motor controller may fail,...

The Issue: The motor controller may fail, which can potentially lead to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...

The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2020· New Standard Device Inc

Recalled Item: 1.8mm Truss Wire Recalled by New Standard Device Inc Due to 1.8mm truss...

The Issue: 1.8mm truss wires are being removed to facilitate the introduction of 2.0mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...

The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· HF Acquisition Co. LLC

Recalled Item: STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: Recalled...

The Issue: A missing component (hand suction pump) in the emergency medical kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component...

The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 6mm implant component...

The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Medtronic Navigation, Inc.

Recalled Item: StealthStation" S7 System with Polaris Spectra Camera part number PSU...

The Issue: There is a potential for specific camera units to be affected by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Verathon, Inc.

Recalled Item: GlideScope Core OneTouch Smart Cable Recalled by Verathon, Inc. Due to When...

The Issue: When video laryngoscopy system users apply, twisting motions while...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2020· Akorn, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· AVKARE Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2020· AVKARE Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund