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. 2,244 recalls have been distributed to Vermont in the last 12 months.
Showing 43561–43580 of 47,027 recalls
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...
The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...
The Issue: Unexpected movement during beam delivery may not be detected if there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...
The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Discoloration: This recall is being carried out due to a yellow to brown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orville Redenbacher's Classic Kettle Korn Recalled by Conagra Inc Due to...
The Issue: The kettle korn flavored ready-to-eat popcorn product may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...
The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Sync C100-Physio Radiotransparent Defibrillation Electrodes Monophasic...
The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...
The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vermed Recalled by Heart Sync, Inc Due to On 4/18/13 HEARTSYNC became aware...
The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...
The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******microMax Handpiece***Rx Only***Manufacturer: The Anspach Effort...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...
The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.