Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,576 recalls have been distributed to Idaho in the last 12 months.
Showing 8041–8060 of 27,833 recalls
Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...
The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with...
The Issue: The automated dispensing cabinet software update included a .dll file that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...
The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283)...
The Issue: It may occur that after system startup no stand movement is possible any...
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 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 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 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 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 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 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: 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 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: 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: 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: 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: 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.
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: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...
The Issue: Complaints relating to urine output measurement accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.