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 23681–23700 of 27,157 recalls
Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products White Slides Recalled by Ortho-Clinical...
The Issue: An incorrect assay value (0.3785) was printed on the product carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Recalled...
The Issue: Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-AB Abdominal Dressing Kit with Soft Port Recalled by...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F XL with Soft Port REF #: Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS Soft Port (The RENASYS Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...
The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...
The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...
The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panaroma Central Station Product Usage: This device can view real time...
The Issue: Mindray has identified two issues with the Panorama Central Station. Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...
The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...
The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular...
The Issue: Defective component may cause extension sets to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Recalled by Roche...
The Issue: Numerous complaints have been filed that leaking cobas ¿ PCR media 4.3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infantino Squeeze & Teethe Monkey Recalled by Infantino LLC Due to Infantino...
The Issue: Infantino initiated this voluntary recall of all lots of Infantino Squeeze &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.