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. 2,521 recalls have been distributed to Vermont in the last 12 months.
Showing 4881–4900 of 27,157 recalls
Recalled Item: MEDLINE BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE BOTTLE KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE TRAY ADULT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofsilk Braided Silk sutures: CS-211 SOFSILK* 4-0 BLK 45CM CVF21 Recalled by...
The Issue: Specific lots of sutures were sterilized with gamma doses that exceeded the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TERUMO HydroPearl Compressible Microspheres for Embolisation Recalled by...
The Issue: Due to, during the manufacturing process, the prescribed manufacturing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide Recalled...
The Issue: When utlizing the patient query feature on the Zyno Medical Z-800WF pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...
The Issue: The firm has become aware of a sudden increase in complaints for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco MDSC-8527 NXF Recalled by Barco N.V. Due to Barco became aware of a...
The Issue: Barco became aware of a problem with I2C cables in the manufacturing process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Medfusion Model 4000 syringe pump Recalled by Smiths Medical...
The Issue: Medfusion Model 4000 syringe infusion pumps, with the following software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...
The Issue: Reason for the voluntary recall is residue was identified on the two forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...
The Issue: When the catheters are used with the EnSiteX EP System, the system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...
The Issue: The jaw may fracture prior to the procedure during the inspection instructed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...
The Issue: Devices may not be rendered sterile due to an internal gap that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.