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. 2,430 recalls have been distributed to Alaska in the last 12 months.
Showing 18901–18920 of 46,762 recalls
Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...
The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by AuroMedics Pharma LLC Due...
The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amantadine Hydrochloride Tablets Recalled by Jubilant Cadista...
The Issue: Presence of Foreign Substance: Presence of a foreign object in a single tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Color Coleslaw - Marketside brand Recalled by Dole Fresh Vegetables Inc...
The Issue: Canadian Food Inspection Agency reported finding Salmonella in a sample of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...
The Issue: The boxes used by the shipper were not validated for use during transport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...
The Issue: Excessive static electricity can potentially cause unrecoverable power loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or...
The Issue: Labeling: Incorrect or Missing Lot and/or expiration date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals, LLC Due to Foreign...
The Issue: Presence of Foreign Substance: Foreign material found inside the vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....
The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.