Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,243 recalls have been distributed to Vermont in the last 12 months.
Showing 46421–46440 of 47,027 recalls
Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...
The Issue: Subpotent Drug: Salicylic acid is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...
The Issue: Subpotent Drug: Salicylic acid is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...
The Issue: Subpotent Drug: Salicylic acid is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...
The Issue: Subpotent Drug: Salicylic acid is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...
The Issue: Subpotent Drug: Salicylic acid is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endocet (oxycodone and acetaminophen) tablets Recalled by Endo...
The Issue: Adulterated Presence of Foreign Tablets: Customer complaint that some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...
The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...
The Issue: Mindray has identified two software anomalies contained in the V Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...
The Issue: The Beauty Angel was marketed without a 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US-001 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance iCT and iCT SP are Computed Tomography X-Ray Recalled by...
The Issue: Philips is issuing a software update (version 3.2.4) to the Brilliance iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 20% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 70% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.