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. 2,400 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,400 in last 12 months

Showing 2142121440 of 48,326 recalls

Medical DeviceMay 30, 2019· Medline Industries, Inc.

Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...

The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...

The Issue: Additional Instructions: step-by step handling and inserting the cassette...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Siemens Healthcare Diagnostics Inc

Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...

The Issue: Potential for increased rate of false positive results and/or increased rate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· AtriCure, Inc.

Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....

The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...

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

Class II — Potential Health HazardOngoing
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-DTPA Kit 10 mg Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Pyrophosphate Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Pentreotide (10 uGm) Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-DMSA solution Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2019· Nobel Biocare Usa Llc

Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...

The Issue: Packaged dental implant healing abutments were found to contain the wrong...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· GN Otometrics

Recalled Item: The ICS CHARTR EP 200 Recalled by GN Otometrics Due to There is a risk to...

The Issue: There is a risk to the healthcare professional or patient of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A...

The Issue: The potential sporadic performance problems may result in scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Zimmer Biomet, Inc.

Recalled Item: DVR Crosslock ePAK Screw Driver Recalled by Zimmer Biomet, Inc. Due to There...

The Issue: There is a potential for weak seals of the sterile packaging.

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

Class II — Potential Health HazardOngoing