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. 1,049 recalls have been distributed to Rhode Island in the last 12 months.
Showing 11781–11800 of 47,970 recalls
Recalled Item: B-Complex + Chromic Chloride (Choline Chloride 3% Recalled by US Specialty...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Homeopathic EarAche Ear Drops Recalled by Grato Holdings, Inc. Due to...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Homeopathic EarAche Drops Recalled by Grato Holdings, Inc. Due to Microbial...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri Ajo King con Ortiga y Omega 3 Tablets Recalled by Walmart Inc Due to...
The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...
The Issue: Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...
The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MiniMed 620G Insulin Pump (O.U.S. version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 740G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 720G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 670G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 640G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G Insulin Pump (U.S. and Canada Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CustMbite Recalled by Dental Choice Holding Llc Due to The device was...
The Issue: The device was marketed and sold in the US without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 770G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System...
The Issue: Potential for stent dislodgement and associated failures related to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis) Recalled by Agilent...
The Issue: Label provided for substrate vail contained incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Item Number: 800774001 Recalled by ROi CPS LLC Due to A nonsterile...
The Issue: A nonsterile component was packaged in a sterile convenience kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Icono Recalled by Siemens Medical Solutions USA, Inc Due to During...
The Issue: During system tests, an increased wearing of the Image acquisition system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.