Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,263 recalls have been distributed to Rhode Island in the last 12 months.
Showing 44561–44580 of 47,970 recalls
Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rostorelle L Recalled by Coloplast Manufacturing US, LLC Due to Mislabeling
The Issue: Coloplast is recalling one lot of Restorelle L prosthesis because it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.