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. 2,525 recalls have been distributed to Vermont in the last 12 months.
Showing 3581–3600 of 27,157 recalls
Recalled Item: BD PYXIS MEDBANK TWR MN CR-14HH-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with...
The Issue: Potential for false negative response on the NIM Vital Nerve Monitoring System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG-410 Electrosurgical Generator- In conjunction with electrosurgical...
The Issue: Electrosurgical Generators ESG-410 does not power on upon use, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...
The Issue: Specimen collection device may leak after the patient sample swabs have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...
The Issue: Potential for defective test cartridges which may result in false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: If blood culture identification panel is used in conjunction with specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...
The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-VU KUMPE 5F X 65CM -Used for patients in need Recalled by...
The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count Recalled by Embecta Corp. Due...
The Issue: BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Handset with Communicator Recalled by Medtronic Neuromodulation...
The Issue: A subset of the handsets within the kit may not be able to complete the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Afinion 2 Analyzer Recalled by Abbott Diagnostics Technologies AS Due to...
The Issue: Five Afinion 2 (AF2) Analyzer were incorrectly market configured as Moderate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Kit containing the Microtek decanter Recalled by ROi CPS LLC Due to...
The Issue: Decanters may have pin holes and tears in sterile packaging that cannot be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an Recalled by B. Braun...
The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusomat UNIV. 15 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.