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 6841–6860 of 27,157 recalls
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size...
The Issue: All lots of BIOSTOP G Bioresorbable Cement Restrictor are being removed as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Flow Disposable Patient Circuit for the Precision Flow System Recalled...
The Issue: There have been reports of excessive condensation associated with certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 4Fr Single Lumen Recalled by Access Vascular, Inc Due to Select...
The Issue: Select catheter lots were identified to be labeled with incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen - Basic Kit Recalled by Access Vascular, Inc Due...
The Issue: Select catheter lots were identified to be labeled with incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 4Fr Single Lumen Recalled by Access Vascular, Inc Due to Select...
The Issue: Select catheter lots were identified to be labeled with incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotome MammoStar Biopsy Site Identified Recalled by Carbon Medical...
The Issue: The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaGuide Intelligent Ultrasound System Recalled by NovaSignal Corp. Due to...
The Issue: Transcranial Doppler/ultrasound system tablet has a faulty hard drive, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Material # Artis zee floor 10094135 Artis zee ceiling Recalled by...
The Issue: In rare cases, the system may only boot into backup mode after an abrupt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lucid TCD 2.0 System Recalled by NovaSignal Corp. Due to Transcranial...
The Issue: Transcranial Doppler/ultrasound system tablet has a faulty hard drive, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Mechanical...
The Issue: Mechanical connection between the tabletop and table base may be lost.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH V+ Spinal Cement System Recalled by TEKNIMED SAS Due to Incorrect...
The Issue: Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative...
The Issue: Leakage of the original specimen from the plastic microfluidic cartridge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Recalled by Biomet, Inc. Due to Packaged in the...
The Issue: Packaged in the incorrect shelf carton. Incorrect shelf carton; outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McCormick Medical Distribution PORT TRAY Recalled by Stradis Healthcare Due...
The Issue: Potential for the outer bag having pinhole leaks near the seal, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCT 12 CC SYRINGE KIT Recalled by Stradis Healthcare Due to Potential for...
The Issue: Potential for the outer bag having pinhole leaks near the seal, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCT 6 CC SYRINGE KIT Recalled by Stradis Healthcare Due to Potential for the...
The Issue: Potential for the outer bag having pinhole leaks near the seal, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stradis Healthcare TCTR Convenience Kit. Manufactured by Stradis Healthcare....
The Issue: Potential for the outer bag having pinhole leaks near the seal, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCT MAX BARRIER PICC INSERTION TRAY 12 per case. Distributed Recalled by...
The Issue: Potential for the outer bag having pinhole leaks near the seal, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.