Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,003 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,003 in last 12 months

Showing 20541–20560 of 48,215 recalls

DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Bimix #3 (Papaverine HCl 30 mg/mL/Phentolamine Mesylate 3 mg/mL) in 5 mL...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Ketamine in 0.9% Sodium Chloride (PF) 10 mg/mL Recalled by KRS Global...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Nicotinamide Adenine Dinucleotide (PF) Recalled by KRS Global Biotechnology,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: fentaNYL Citrate in 0.9% Sodium Chloride (PF) Recalled by KRS Global...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Hydroxocobalamin 10 mg/20 mL (0.5 mg/mL) 20 mL fill in a 30 mL Vial Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: fentaNYL Citrate in 0.9% Sodium Chloride (PF) 2 Recalled by KRS Global...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: OxyTOCIN in 0.9% Sodium Chloride Solution (PF) Recalled by KRS Global...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Recalled by KRS Global Biotechnology, Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2019· Olympus Corporation of the Americas

Recalled Item: Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System -...

The Issue: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Merit Medical Systems, Inc.

Recalled Item: Custom Sheath Introducer Kit - Product Usage: intended Recalled by Merit...

The Issue: labeling error: Due to a manufacturing issue, product package was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Tocotransducer (Nautilus) 2264LAX Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M1356A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco MP Transducer (M2734B) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...

The Issue: Due to low Quality Control recovery and invalid Calibration.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V680 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...

The Issue: Due to low Quality Control recovery and invalid Calibration.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M2736A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing