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. 2,258 recalls have been distributed to Alaska in the last 12 months.
Showing 43281–43300 of 46,762 recalls
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...
The Issue: Subpotent Drug: The products were below specification for potency at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...
The Issue: Subpotent Drug: The products were below specification for potency at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...
The Issue: Subpotent Drug: The products were below specification for potency at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...
The Issue: Subpotent Drug: The products were below specification for potency at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...
The Issue: Subpotent Drug: The products were below specification for potency at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...
The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....
The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...
The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...
The Issue: Unexpected movement during beam delivery may not be detected if there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...
The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Discoloration: This recall is being carried out due to a yellow to brown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.