State
73,566 recalls have nationwide distribution and so reach Idaho. 3,523 additional recalls listed Idaho specifically in their distribution scope.
Of the 3,523 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,217 (35%) are Severe.
Which agencies issued them
These figures cover only the 3,523 recalls whose distribution notice names Idaho specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
NSE Products, Inc. is recalling Pharmanex Kids Jungamals dietary supplement because the label does not disclose fish allergen present in the product's Vitamin E ingredient.
Lupin Pharmaceuticals is recalling Irbesartan 75 mg tablets due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient. The recall affects 51,144 bottles distributed nationwide.
GM Helix Acqua Implant dental implants were mislabeled as a smaller size. If incorrectly installed in cases with low bone quality, they could damage the nerve or adjacent bone structures.
Implant Direct Sybron Manufacturing is recalling 83 dental implants from lot 166300 because the implants differ in size from what is labeled on the packaging. The implants were distributed across multiple US states and Japan.
ABUS is recalling about 790 MountZ youth helmets that do not meet U.S. safety standards for bicycle helmets. The helmets pose a risk of head injury and should be returned for a full refund.
Implant Direct is recalling 61 dental implants because the packaged implants are a different size than declared on the labeling. Patients who may have received these implants should contact their healthcare provider.
Bayer Medical Care is recalling 6,950 units of MEDRAD Twist & Go Disposable Syringes due to labeling errors that could cause confusion about syringe compatibility with the MEDRAD Mark 7 Arterion Injection System.
Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/80 mg) because the product was manufactured using an excipient that failed to meet conductivity specifications.
PepsiCo is recalling Starbucks Doubleshot Espresso canned coffee products due to inadequate sealing that may lead to premature spoilage. The recall affects approximately 85,956 cases distributed nationwide.
Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/20 mg) nationwide because the product was manufactured using an excipient that failed conductivity specifications.
Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/40 mg tablets because an excipient used in manufacturing failed conductivity specifications. The recall affects 11,590 bottles of 30-count and 3,585 bottles of 90-count packages distributed nationwide.
MicroVention's Aspiration Syringe Kit (REF: MVSK60) was labeled for international distribution but inadvertently shipped to U.S. customers. The affected lot (H2146461) was distributed to Alabama, Nevada, and New York.
Dr. Reddy's Laboratories is recalling 696 bottles of Ezetimibe and Simvastatin Tablets (10 mg/40 mg) distributed nationwide due to failed excipient specifications and the presence of foreign tablets in bottles.
Lupin Pharmaceuticals is recalling Irbesartan 300 mg tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects approximately 119,544 bottles distributed nationally.
Medtronic recalled the Clinician Programmer Application (CPA) model A610 due to a potential software anomaly. Affected versions 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081 have been distributed worldwide. No illnesses or injuries have been reported.
Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/10 mg tablets nationwide because the product was manufactured using an excipient that failed to meet conductivity specifications.
PepsiCo is recalling Starbucks Doubleshot Espresso and Espresso & Cream canned coffee products because inadequate sealing may cause premature spoilage.
PepsiCo is recalling Starbucks Doubleshot Espresso and Espresso & Salted Caramel Cream canned coffee products due to inadequate sealing that may lead to premature spoilage.
Tesla is recalling certain 2021 Model X and Model S vehicles because the driver's air bag cushion may tear during deployment, potentially failing to protect occupants in a crash. Tesla will replace the air bag free of charge.
Keystone RV Company is recalling 2022 Arcadia fifth wheel travel trailers because the Federal Identification Label contains incorrect tire size and pressure information. This could lead to over-inflation and increase the risk of crashes.
Autocar is recalling 2019-2022 Xpeditor vehicles because the hazard lights will not function with the ignition turned off. This violates federal safety standards and could increase crash risk in hazard situations.
Isuzu is recalling 2018-2021 FTR and Chevrolet 6500XD trucks because a steering bolt may loosen, causing difficulty steering and increased crash risk.
2021-2022 Western Star 49X trucks may have improperly installed steering shafts that can separate, causing loss of steering control. Daimler will inspect and repair affected vehicles free of charge.
Kia Motors America is recalling 2020-2021 Stinger vehicles with a fuel gauge software error that may cause inaccurate readings, risking unexpected fuel depletion and vehicle stalling.
Yamaha is recalling 2016-2021 FJR1300 motorcycles because a previous software update may prevent the engine from accelerating as intended, increasing crash risk.