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. 2,295 recalls have been distributed to Vermont in the last 12 months.
Showing 36921–36940 of 47,027 recalls
Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Southwestern 4oz Veggie Burger 36 count Net Wt 9 lb. Recalled by Cuisine...
The Issue: Products may contain cumin which may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chef's Line Black Bean Burger 36-4.25 oz Net Wt. 9 Recalled by Cuisine...
The Issue: Products may contain cumin which may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rugby Poly Vitamin Liquid Recalled by Pharmatech Llc Due to Packaging label...
The Issue: Packaging label does not match individual product labeling. Outside...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Guiltless Gourmet Southwestern Veggie Burger 2.5oz 48 pieces Distributed by:...
The Issue: Products may contain cumin which may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rugby Poly Vitamin Liquid with Iron Recalled by Pharmatech Llc Due to...
The Issue: Packaging label does not match individual product labeling. Outside...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Black Bean Burger 4.5 oz 40 pieces Net Wt. 11.25 Recalled by Cuisine...
The Issue: Products may contain cumin which may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a Recalled...
The Issue: Fujifilm is reporting a corrective action due to an FDA inspection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product...
The Issue: Fujifilm is conducting a corrective action due to an FDA inspection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gemini 16 PET/CT System (Uninterruptible Power Supply (UPS) accessory...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...
The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X (Uninterruptible Power Supply (UPS) accessory devices) Computed...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 6.x. is software used to place patients at an Recalled by Brainlab...
The Issue: ExacTrac 6.x Patient Positioning System: Potentially incorrect patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core (Uninterruptible Power Supply (UPS) accessory devices)...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex (Uninterruptible Power Supply (UPS) accessory devices)...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gemini GXL 16 Slice (Uninterruptible Power Supply (UPS) accessory devices)...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 6 Slice Air (Uninterruptible Power Supply (UPS) accessory...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Slice Air (Uninterruptible Power Supply (UPS) accessory...
The Issue: The firm was notified that the failure of the UPS accessory devices used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YC-1800 OPHTHALMIC YAG LASER SYSTEM Recalled by Nidek Inc Due to Dear Doctor...
The Issue: Dear Doctor letter and Quick Guide is being sent to users of the YC-1800 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.