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. 1,027 recalls have been distributed to Alaska in the last 12 months.
Showing 14821–14840 of 46,762 recalls
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...
The Issue: Claim for stability after reconstitution from lyophilized to liquid form...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...
The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Vanilla Bean Plant-Based Protein Shake Recalled by Pepsico Inc Due to...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Double Chocolate Plant-Based Protein Shake Recalled by Pepsico Inc...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Electrostatic Filter Angled Recalled by Covidien, LP Due to The company was...
The Issue: The company was notified by their supplier of sterilization services for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB10R94R6 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB7J98R7 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB4W67R20 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB7J97R8 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10R79R6 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB11J14R2 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.