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. 2,435 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,435 in last 12 months

Showing 1808118100 of 46,762 recalls

DrugMarch 11, 2020· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2020· Boddingtons Plastics Ltd

Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...

The Issue: Updated Instructions For Use- to contraindications and potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Skytron, Div. The KMW Group, Inc

Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...

The Issue: Intermittent failure of a signal being sent to a monitor from the touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...

The Issue: As part of an investigation into a biocompatibility test discrepancy where a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...

The Issue: The specified reagent packs exhibit an increase in the frequency of...

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

Class III — Low RiskOngoing
Medical DeviceMarch 10, 2020· Radiometer Medical ApS

Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...

The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Sotalol HCL Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of particulate matter. presence of metal particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Sun Pharmaceutical Industries, Inc....

The Issue: Presence of foreign substance: Foreign matter has been identified as latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 9, 2020· Medline Industries Inc

Recalled Item: Custom convenience kits containing Medline brand Sterile Pre-Saturated...

The Issue: Medline identified that there may be a potential for voids in the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor UPN: M006192132080...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .0383CM FLEX ANG/150CM UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX /150CM Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Abbott Gmbh & Co. KG

Recalled Item: ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25. Recalled by Abbott Gmbh...

The Issue: An erroneous concentration value for hepatitis A virus was utilized during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .038 3CM FLEX STR/150CM Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing