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. 1,968 recalls have been distributed to Alaska in the last 12 months.
Showing 4841–4860 of 46,762 recalls
Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...
The Issue: Incorrect GTIN number on carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance CS2 and Avance CS2 Pro. These anesthesia gas machines Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7100 Recalled by Datex-Ohmeda, Inc. Due to Potential issue that may...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Umary Acido Hialuronico Recalled by SoloVital Due to Undeclared Diclofenac
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gold Hard Steel Plus Liquid Recalled by Supercore Products Group Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Steel Capsules packaged in 1 count blister packs in boxes of 10...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elin Dessert Plates. The recalled plates are lilac in color with orange...
The Issue: Elevated levels of cadmium in plates
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Al'Fez Natural Tahini in 5.6oz glass jars Recalled by AB WORLD FOODS US INC...
The Issue: Potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo Pharmaceuticals,...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...
The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: Due to a software issues, after the instrument processes 250 racks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS XT Chemistry Products ALB-TP Slides is a single Recalled by...
The Issue: The reason for this recall is QuidelOrtho has determined that during normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covideien McGRATH MAC Video Laryngoscope Recalled by Covidien Due to IFU...
The Issue: IFU update to address device's battery handling information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH" MAC EMS Video Laryngoscope Recalled by Covidien Due to Battery...
The Issue: Battery management system within Laryngoscope devices may deplete below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 2 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 4 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BKIT BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.