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 24281–24300 of 27,157 recalls
Recalled Item: PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower...
The Issue: PENTAX Medical has become aware of a product issue associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR ActiveTrak Excimer Laser System Recalled by Abbott Medical Optics, Inc....
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: OSOM C. Difficile Toxin A/B Test Catalog Numbers: Recalled by...
The Issue: Sekisuki Diagnostics has issued a Product Correction for certain lot numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System with Variable Spot Scanning Recalled by Abbott...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...
The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...
The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....
The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...
The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...
The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira has become aware of customers using the incorrect size Receptal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.