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 10841–10860 of 46,762 recalls

DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Whitening Mouthwash Recalled by Family Dollar Stores, Llc. Due to...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Trisodium Citrate 0.5% Solution Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-0.125% Bupivacaine HCl Injection Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2022· Nephron Sc Inc

Recalled Item: Ketorolac Tromethamine Injection Recalled by Nephron Sc Inc Due to cGMP...

The Issue: cGMP Deviations: deviations leading to potential cross-contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2022· Hologic, Inc

Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...

The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...

The Issue: Firm noted an increase in customer reports of leaks.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: Burns of varying degrees can occur to patients with electrodes left in while...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2022· Akorn, Inc

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...

The Issue: Identification of an unknown impurity at the 12-month stability point....

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· LNK International, Inc.

Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...

The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2022· Eclectic Institute Inc

Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...

The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System Recalled by Merit Medical Systems, Inc. Due to Biopsy...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing