Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1596115980 of 46,762 recalls

Medical DeviceDecember 11, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products CKMB Slides: (1)VITROS CKMB Slides (60 Slide...

The Issue: VITROS Chemistry Products CKMB Slides Potential for Falsely Elevated Results...

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

Class II — Potential Health HazardOngoing
DrugDecember 10, 2020· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...

The Issue: Subpotent Drug: Low out-of-specification assay results for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 10, 2020· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 600FP Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Clerio Vision

Recalled Item: Clerio Vision Recalled by Clerio Vision Due to One lot of contact lenses...

The Issue: One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Accuray Incorporated

Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...

The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2020· Accuray Incorporated

Recalled Item: TomoTherapy Treatment System - Product Usage: used as an integrated Recalled...

The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...

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

Class II — Potential Health HazardOngoing
DrugDecember 9, 2020· Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 9, 2020· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Hydroxyzine Hydrochloride Oral Solution Recalled by Morton Grove...

The Issue: Failed Impurities/Degradation Specification: OOS for the following - unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 9, 2020· Biogen MA Inc.

Recalled Item: Vumerity (diroximel fumarate) delayed-release capsule Recalled by Biogen MA...

The Issue: Failed dissolution specifications: out-of-specification test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Imatinib Mesylate Tablets 400 mg Recalled by Shilpa Medicare Limited Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Docetaxel Injection USP 160 mg/8mL (20 mg/mL) Recalled by Shilpa Medicare...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Busulfan Injection 60 mg/10 mL (6 mg/mL) Recalled by Shilpa Medicare Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 8, 2020· Shilpa Medicare Limited

Recalled Item: Imatinib Mesylate Tablets 100 mg Recalled by Shilpa Medicare Limited Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization...

The Issue: System table may tilt because the bolts that fasten the vertical column and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization...

The Issue: System table may tilt because the bolts that fasten the vertical column and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization...

The Issue: System table may tilt because the bolts that fasten the vertical column and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· PHILIPS HOME HEALTHCARE SOLUTION

Recalled Item: ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system Recalled by...

The Issue: After the user selects the Lock-in command, the kV and mA values are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC-107: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing