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. 2,572 recalls have been distributed to Idaho in the last 12 months.
Showing 9561–9580 of 27,833 recalls
Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....
The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...
The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...
The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...
The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...
The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...
The Issue: Elevated rates of false negative results may occur when using blood culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit Catalog Number 70-6762 Recalled by Magellan...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x22x15mm Catalog Number: 6101-2102215NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriIFit TS SIZE 2 Recalled by Corin Ltd Due to Units from one batch of...
The Issue: Units from one batch of TriFit TS size 2 stem were found to be labeled as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit CF SIZE 7 Recalled by Corin Ltd Due to Units from one batch of...
The Issue: Units from one batch of TriFit TS size 2 stem were found to be labeled as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear....
The Issue: Potential that a limited number of individual contact lens packages have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnera 400A Digital Radiographic System Recalled by Arcoma AB Due to There...
The Issue: There is the potential for the X-Ray system to short circuit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnera 400T Digital Radiographic System Recalled by Arcoma AB Due to There...
The Issue: There is the potential for the X-Ray system to short circuit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System...
The Issue: Due to a software error, the user may lose functionality of the system or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WorkMate Claris v.1.2 Upgrade Kits Recalled by Abbott Laboratories Inc. (St...
The Issue: Due to a software error, the user may lose functionality of the system or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System...
The Issue: Due to a software error, the user may lose functionality of the system or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.