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. 2,376 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,376 in last 12 months

Showing 2488124900 of 48,326 recalls

Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2018· General Mills, Inc

Recalled Item: Cheerios Protein Oats & Honey Recalled by General Mills, Inc Due to...

The Issue: Cheerios Protein Oats and Honey cereal may be contaminated with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 13, 2018· Pepsico Inc

Recalled Item: Diet Pepsi 7.5 oz cans Recalled by Pepsico Inc Due to Undeclared Aspartame

The Issue: Diet Pepsi 7.5 oz cans, 6 pack, are recalled due to undeclared Aspartame.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...

The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Haemonetics Corporation

Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...

The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...

The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Smiths Medical ASD Inc.

Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...

The Issue: The product was mislabeled with the incorrect label.

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

Class III — Low RiskOngoing
Medical DeviceJuly 13, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...

The Issue: Analyzers were distributed with software which lacks a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Haemonetics Corporation

Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...

The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set Recalled by Medical...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: DUO FLOW CUSTOM TRAYS Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow XTP Straight Full Set Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: DUO FLOW DOUBLE LUMEN CATHETER Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow IJ Full Tray Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Double Lumen CRRT/ABP Catheter Set Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing