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. 2,257 recalls have been distributed to Vermont in the last 12 months.
Showing 41121–41140 of 47,027 recalls
Recalled Item: Lemon Butter Cookies sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Double Chocolate Butter Cookies sold under the Lambs Farm brand Recalled by...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheerful Cookie Combo containing an assortment of Lemon Butter Cookies...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Famous Butter Cookies sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCHESTRA/ORCHESTRA PLUS Programmer Recalled by Sorin Group Italia S.r.l....
The Issue: Sorin has voluntarily issued a notification to physicians related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71058-XX: 04.2mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: lM71059-XX: Indus Screw 04.2mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71016-XX: 04.5mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro clear(R) 1 day Sphere (o mafilcon A) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight(TM) Toric 1 day (ocufilcon D) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: vitaliKOR Ready When You Are Recalled by Vitality Research Labs LLC Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: P-BOOST Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURECT Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.