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. 2,508 recalls have been distributed to Vermont in the last 12 months.
Showing 6741–6760 of 27,157 recalls
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1)...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml Recalled by...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Recalled...
The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...
The Issue: Product is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN Protein C 5 kit is for in vitro quantitative Recalled by Aniara...
The Issue: New warnings and precautionary statements on product labelling: Reagent 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...
The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...
The Issue: Siemens Healthineers has received customer complaints and confirmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...
The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog...
The Issue: Product did not meet shelf-life testing requirements resulting in a breach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...
The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...
The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Triglycerides_2: in vitro diagnostic use in the quantitative...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N)...
The Issue: An increased incidence of damage to the nut band from a new vendor (Boamax)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)...
The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens...
The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.