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. 2,369 recalls have been distributed to Vermont in the last 12 months.
Showing 19261–19280 of 27,157 recalls
Recalled Item: Various trauma and sports medicine instruments and implants. Plate Recalled...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. guide Recalled...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Reamer....
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Bit Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Spinal...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item 3456103A The...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Fastener...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Screw Recalled...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Rod Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Recalled by B...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...
The Issue: Reports of failure of the device's power supply.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 5 mm x 13 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...
The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...
The Issue: Report of unintentional movement of table to reverse tilting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/2" x 1.5" : 20-06S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...
The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mass Eye & Ear Finger Cot Nasal 2's : Recalled by American Surgical Company...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Tonsil Sponges 1" Large : 50-01 Product Recalled by...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.