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. 2,322 recalls have been distributed to Vermont in the last 12 months.
Showing 32001–32020 of 47,027 recalls
Recalled Item: Brussels Sprouts Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...
The Issue: Brussels Sprouts are recalled because they have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Root Medley Recalled by CRF Frozen Foods, LLC Due to Potential...
The Issue: Organic Root Medley is recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mini Bow Tie Pasta and Vegetable Blend Recalled by CRF Frozen Foods, LLC Due...
The Issue: Mini Bow Tie Pasta and Vegetable Blend is recalled because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...
The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...
The Issue: Defective Delivery System: Defective stem valve causes leakage of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...
The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Linezolid Injection Recalled by Teva North America Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Due to potential for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norditropin FlexPro Somatropin (rDNA origin) injection Recalled by Novo...
The Issue: Defective Delivery System; may have a low frequency assembly fault which may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...
The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5 Recalled by Volcano Corporation Due to Volcano has become aware...
The Issue: Volcano has become aware of an incompatibility issue between Impacted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...
The Issue: It has been found that if the scan range extends beyond the maximum Field of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.