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. 1,057 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,057 in last 12 months

Showing 6721–6740 of 46,762 recalls

DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Walgreens Dye-Free Magnesium Citrate Saline Laxative/Oral Solution Recalled...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Recalled Item: Americaine Recalled by Insight Pharmaceuticals LLC, a Prestige Consumer...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pfizer Inc.

Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; identified as glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Good Neighbor Pharmacy Recalled by Pharma Nobis LLC Due to MICROBIAL...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2023· Lupin Pharmaceuticals Inc.

Recalled Item: Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and Recalled...

The Issue: CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 20, 2023· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide Recalled...

The Issue: When utlizing the patient query feature on the Zyno Medical Z-800WF pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· CooperSurgical, Inc.

Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...

The Issue: The firm has become aware of a sudden increase in complaints for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2023· Barco N.V.

Recalled Item: Barco MDSC-8527 NXF Recalled by Barco N.V. Due to Barco became aware of a...

The Issue: Barco became aware of a problem with I2C cables in the manufacturing process...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· Acumed LLC

Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2023· Smiths Medical ASD Inc.

Recalled Item: smiths medical Medfusion Model 4000 syringe pump Recalled by Smiths Medical...

The Issue: Medfusion Model 4000 syringe infusion pumps, with the following software...

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

Class I — Serious Health HazardOngoing
FoodDecember 19, 2023· Houdini Inc.

Recalled Item: Ministry of Snacks Sweet and Savory Collection #8700 Recalled by Houdini...

The Issue: Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 18, 2023· Vortex Surgical Inc.

Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...

The Issue: Reason for the voluntary recall is residue was identified on the two forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2023· St. Jude Medical, Atrial Fibrillation Division, Inc.

Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...

The Issue: When the catheters are used with the EnSiteX EP System, the system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Olympus Corporation of the Americas

Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...

The Issue: The jaw may fracture prior to the procedure during the inspection instructed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...

The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2023· Philips North America

Recalled Item: BrightView Recalled by Philips North America Due to Detector may...

The Issue: Detector may unexpectedly fall due to a component failure. If the detector...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2023· Hologic, Inc.

Recalled Item: PANTHER FUSION System The Panther System is an Recalled by Hologic, Inc. Due...

The Issue: Due to potential false positive Flu B results when a sample was also...

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

Class II — Potential Health HazardOngoing