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. 983 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
983 in last 12 months

Showing 27981–28000 of 48,215 recalls

DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Phenylephrine HCL in 0.9% Sodium Chloride 10 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: NORepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg)...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....

The Issue: A software issue may result in the previous settings being applied instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...

The Issue: A software issue may result in the previous settings being applied instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Panoramic Rental Corp.

Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...

The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Microline Surgical, Inc.

Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...

The Issue: The heat-shrink insulation tube may split during autoclave...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Bios S.r.l.

Recalled Item: THERMI250 Radiofrequency System. Intended to provide heating for the purpose...

The Issue: In some systems, the unit continues to emit RF energy after the PAUSE button...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2017· Medtronic Vascular Galway DBA Medtronic Ireland

Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...

The Issue: Stylette removal difficulties on the Euphora and Solarice products.

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2017· Pfizer Inc.

Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...

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

Class III — Low RiskOngoing
Refund