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. 2,544 recalls have been distributed to Idaho in the last 12 months.
Showing 14401–14420 of 48,215 recalls
Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage Recalled by Revive...
The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artesunate for Injection Recalled by AMIVAS (US), LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Air filter failed post integrity test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES Recalled by O&M...
The Issue: All lots of the glove may discolor and lose elasticity upon aging, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...
The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...
The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil TiLite Recalled by TiSport, Llc Due to Some affected wheelchairs,...
The Issue: Some affected wheelchairs, with transit tie downs, that are used as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-Ray System Recalled by Philips...
The Issue: When the user presses or releases both the APC (accept) button and the Float...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error, the software can produce an incorrect interpretation of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...
The Issue: A software anomaly may occur with the clinician programmer application.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...
The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.