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 14461–14480 of 48,215 recalls
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5MMX165MM CANNULATED SCREW Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The product label incorrectly indicated that the screws are fully threaded,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlipiZIDE Extended-Release Tablets Recalled by American Health Packaging Due...
The Issue: Failed Dissolution Specifications: results were above specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Injection Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Defective container: Cracked vials leading to lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIO-RAD BioPlex 2200 SYPH T PACK Syphilis Total Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Medical Linear Accelerator (EMLA) Recalled by Elekta, Inc. Due to...
The Issue: There is a risk that the Diode D1 in the Modulator can fail in a destructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valproic Acid Oral Solution Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The MEDRAD Twist & Go Disposable Syringe 150 mL with Recalled by Bayer...
The Issue: Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Monaco - Product Usage: used to make treatment plans Recalled by...
The Issue: Contour changes can be saved on an unintended image set. In addition, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Bio-Medicus Insertion Kits Recalled by Medtronic Perfusion Systems...
The Issue: There was a label mix-up between two model numbers resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCH Leg Positioning System Recalled by Innovative Orthopedic Technologies,...
The Issue: Due to the holes not being bored to the specific diameter, the locking pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocuronium Bromide Injection 50mg/5 mL Recalled by Piramal Critical Care,...
The Issue: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Pack Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrial Biopsy Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.