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. 2,614 recalls have been distributed to Idaho in the last 12 months.
Showing 1501–1520 of 27,833 recalls
Recalled Item: UROSKOP Omnia Max. Model Number: 10762473 Recalled by Siemens Medical...
The Issue: A resistor in the frequency inverter may strongly overheat potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...
The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...
The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...
The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medshape Universal Joints Recalled by Medshape, INC. Due to Bone external...
The Issue: Bone external fixation system may have the pin that can become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Recalled...
The Issue: Due to a risk of false positive results that could lead to unnecessary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd....
The Issue: Kit USB flash drive contains outdated software, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva IT Nova Product Number: 781175 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.