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 24261–24280 of 47,027 recalls
Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is Recalled...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...
The Issue: An incorrect control board and firmware installed in some of the Hand Held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal...
The Issue: The recalled dietary supplement has the potential to contain undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sisel Recalled by Sisel International Llc Due to Firm is recalling SiselRipt...
The Issue: Firm is recalling SiselRipt due to the presence of an unapproved artificial...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wish Bone House Italian Salad Dressing 15 oz. Recalled by Pinnacle Food...
The Issue: The recall was initiated after learning from a retail customer that a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...
The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...
The Issue: Microbial Contamination of Sterile Products: Product associated with reports...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...
The Issue: Subpotent Drug and Failed Content Uniformity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...
The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.