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. 2,503 recalls have been distributed to Vermont in the last 12 months.
Showing 7441–7460 of 27,157 recalls
Recalled Item: B. Braun CARESITE Port Access Kit w/Tegaderm Recalled by Medical Action...
The Issue: The kits were incorrectly labeled with an extended expiration date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESITE SMALLBORE EXT SET T-PORT 5 IN. Recalled by B. Braun Medical, Inc....
The Issue: The extension set has a high probability of potential failure which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRASITE US04TL Smallbore T-Port Extension Set Recalled by B. Braun...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Tube Sodium Fluoride: 100 mg Recalled by Becton Dickinson &...
The Issue: The affected product contains isobutylene which has recently demonstrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Set Recalled by B. Braun Medical, Inc. Due to The extension set...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to A part defect...
The Issue: A part defect with the wash 1 syringe of an SARS-CoV-2 assay could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit...
The Issue: Mislabeling: the corrugate label, lidstock, banner card, and peel sticker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex HF20 Set (product code 109841). For use in providing Recalled by...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex ST Set: ST60 (product code 107643) Recalled by Baxter Healthcare...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex M Set: M60 (product code 106696) Recalled by Baxter Healthcare...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex M Set: M150 (product code 109990). For use in Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex HF Set: HF1000 (product code 107140) Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 Regular whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.0 whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G041 POD Recalled by Thor Photomedicine Ltd Due to Failure of ball stud...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 XL whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADLT BLOOD CLUTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PHERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756 Recalled by MEDLINE...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.