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 25321–25340 of 27,157 recalls
Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...
The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (100 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Vitamin D Assay (500 tests) Recalled by Siemens Healthcare...
The Issue: Negative bias in patient samples for Vitamin D
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...
The Issue: This recall is being initiated because the affected lots of this product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...
The Issue: GE Healthcare has become aware of a potential safety issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...
The Issue: Philips Healthcare received a report from the field stating when they viewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...
The Issue: The firm received complaints for unintended movements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....
The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms....
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood and Recalled by Becton...
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Perinatal and Centricity Intensive Care is intended to be...
The Issue: 1) Under rare network conditions, a Centricity Perinatal process may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood. Used Recalled by...
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All OneTouch Verio IQ Blood Glucose Meters sold as: Verio Recalled by...
The Issue: The Verio IQ meter will shut off and revert to set up mode at glucose values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the Recalled by...
The Issue: Siemens has observed that the listed lot numbers show an increase in Heparin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 Recalled by...
The Issue: Recall is being initiated due to the part being mislabeled (Part Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Recalled by...
The Issue: Ormco Corporation is voluntarily recalling one (1) lot of Bracket Buccal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Systems with Software Artis VC20x/VC21A/VD10x that have a DSA Recalled...
The Issue: The firm has become aware of a potential issue on Artis systems with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICYCL-E- Lite Portable Oxygen System An integrated portable oxygen...
The Issue: A number of MEDICYL-e Portable Oxygen Systems may have misapplied valve flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture Recalled by...
The Issue: A post market safety review following several customer complaints indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APLIF Implants and Instruments Recalled by Spinal Solutions, LLC Due to...
The Issue: Spinal Solutions is recalling the APLIF system because it is not supported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.