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. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 26301–26320 of 47,027 recalls
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Incision and Drainage Tray Kit Recalled by Medline Industries Inc...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Concordia Trunk Kit. Packaged for Medline Industries Recalled by...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aplicare Povidone-Iodine Prep Pad Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Pediatric IV Kit. Packaged in USA for Medline Industries Recalled by...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinonide Gel USP Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross contamination with other products: traces of Dapsone were found in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...
The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Death Wish Nitro Canned Cold Brew Coffee 11 oz Recalled by Death Wish Coffee...
The Issue: Potential for Clostridium Botulinum
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RHINO 7 Platinum 5000 Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intralipid 20% Recalled by Baxter Healthcare Corporation Due to Temperature...
The Issue: Temperature Abuse: A portion of this product lot was exposed to subfreezing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.