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. 1,762 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,762 in last 12 months

Showing 3700137020 of 48,215 recalls

DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Estradiol 18 mg Recalled by The Compounding Pharmacy of America Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: MEGA-BURN III Injection Recalled by The Compounding Pharmacy of America Due...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Testosterone 60 mg Recalled by The Compounding Pharmacy of America Due to...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: DMPS (Sodium 2 Recalled by The Compounding Pharmacy of America Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Hydroxocobalamin 5 Recalled by The Compounding Pharmacy of America Due to...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Alprostadil 40 mcg/ml Injection Recalled by The Compounding Pharmacy of...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Testosterone 62.5 mg Pellet Recalled by The Compounding Pharmacy of America...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Estradiol 4 mg Recalled by The Compounding Pharmacy of America Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2015· ArthroCare Corporation

Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...

The Issue: Wands inspected with the adaptor fixture were released to the field not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...

The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· Alcon Research, Ltd.

Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...

The Issue: Insufficient seal on the outside packaging, potentially affecting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Optical Access System Recalled by Stryker Sustainability Solutions Due to...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Fios First Entry Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing