The Recall Desk

State

Idaho product recalls

20,364 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho specifically in their distribution scope.

About recalls in Idaho

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Idaho consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15751–15775 of 20364

  • HighFDA (Devices)·Z-1647-2022·2022-09-07

    Siemens Artis icono X-Ray Systems Recalled for Potential Hardware Failure

    Siemens has recalled Artis icono X-ray imaging systems due to a potential hardware issue affecting a specific lot of X-ray tubes. If the error detection mechanism fails, the system cannot release X-rays until it is shut down.

    Product
    Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1682-2022·2022-09-07

    Sweetums Sucrose Solution Recalled for Contamination and Leaking Cups

    Clinical Innovations is recalling Sweetums 24% Sucrose Solution used in NICU settings due to leaking cups and black particulates in the solution. The recall affects 1,773 boxes distributed nationwide.

    Product
    Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptically packaged in 15 mL cups with foil lid. Each cup contains 15 mL of USP purified water, 24% sugar, citric acid (buffer). Cup is latex-free, DEHP-free, BPA-fr
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2022·2022-09-07

    ARCHITECT STAT Troponin-I Reagent Kit Recalled for Insufficient Blocking Agents

    Abbott is recalling one lot of ARCHITECT STAT Troponin-I Reagent Kits due to insufficient heterophilic blocking agents in the conjugate, which may affect test accuracy.

    Product
    ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1468-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions

    Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1466-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions

    Colgate Anticavity Fluoride Toothpaste, Optic White Renewal was recalled after being stored outside appropriate temperature conditions. The recall affects 840 packages distributed to Family Dollar stores in 11 states.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITTE RENEWAL, 3% Hydrogen Peroxide, High Impact White, Net Wt. 3.0 OZ. (85 g) UPC 0 35000 97008 4. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1668-2022·2022-09-07

    DeRoyal Sterile Custom Kits Recalled for Defective Connectors

    DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors are being recalled because the procedure packs contained a recalled product. Approximately 1,306 kits were distributed in Ohio and Tennessee.

    Product
    DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1472-2022·2022-09-07

    Nighttime Sleep-Aid tablets recalled due to carton labeling error

    CVS Pharmacy is recalling Nighttime Sleep-Aid tablets because the carton incorrectly identifies the active ingredient as doxylamine succinate HCl instead of doxylamine succinate. Approximately 257,064 cartons were distributed nationwide.

    Product
    Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 34873 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1467-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions

    Colgate Anticavity Fluoride Toothpaste OPTIC WHITE ADVANCED ICY FRESH is recalled due to improper temperature storage during manufacturing. Approximately 1,680 packages distributed across 11 U.S. states are affected.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE ADVANCED ICY FRESH, Net Wt. 3.2 OZ. (90 g) UPC 0 35000 97159 3. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1646-2022·2022-09-07

    X-ray imaging system hardware defect may prevent operation

    Siemens is recalling certain X-ray imaging systems due to a potential hardware issue with the error detection mechanism. In rare cases, this could prevent X-ray emission until system shutdown.

    Product
    Artis pheno- Model No. 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1469-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste Recalled Due to Improper Storage Conditions

    Family Dollar Stores recalls 1,400 packages of Colgate Anticavity Fluoride Toothpaste due to improper temperature storage conditions during manufacturing. The product may not meet quality standards.

    Product
    Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT PASTE. Net Wt. 4.2 OZ. (119 g) UPC 0 35000 45836 0. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1497-2022·2022-09-07

    Triamcinolone Acetonide Cream Recalled for Manufacturing Defects

    Padagis US LLC is recalling 57,816 tubes of Triamcinolone Acetonide Cream 0.1% nationwide due to manufacturing process deviations. Consumers reported gritty texture and reduced effectiveness.

    Product
    TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1470-2022·2022-09-07

    Colgate OPTIC WHITE Mouthwash Recalled Due to Improper Storage Conditions

    Family Dollar is recalling Colgate Whitening Mouthwash OPTIC WHITE ICY FRESH MINT due to temperature storage deviations. 840 packages were distributed to Family Dollar stores in multiple states.

    Product
    Colgate Whitening Mouthwash, OPTIC WHITE ICY FRESH MINT. 16 fl. OZ. (1 pt) 473 mL UPC 0 35000 67111 0. Dist. by: Colgate-Palmolive Co. New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1471-2022·2022-09-07

    Timolol Maleate eye drops recalled for unknown impurity in stability testing

    Akorn, Inc. is recalling Timolol Maleate Ophthalmic Solution due to identification of an unknown impurity during 12-month stability testing. No illnesses have been reported.

    Product
    Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials, Rx Only, Sterile, Manufactured for: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-189-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V407000·2022-09-06

    2022 RAM Pickup Trucks Recalled for Rearview Camera Display Failure

    Certain 2022 RAM 1500, 2500, and 3500 pickup trucks may have defective radio software that prevents the rearview camera image from displaying, reducing rear visibility and increasing crash risk.

    Product
    RAM — 2022 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V313000·2022-09-05

    2023 Winnebago Ekko RV Recalled for Cracked LP Gas Fittings

    Winnebago is recalling 2021-2023 Ekko recreational vehicles because quick disconnect fittings in the LP gas system may crack, potentially causing a gas leak that could lead to fire.

    Product
    WINNEBAGO — 2023 WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V374000·2022-09-05

    2021 Forest River Columbus Trailer Brakes May Fail Due to Wiring Defect

    Forest River is recalling 2021 Columbus Fifth Wheel trailers due to an incorrectly wired breakaway switch that may prevent the trailer brakes from activating, increasing the risk of crashes.

    Product
    FOREST RIVER — 2021 FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V317000·2022-09-05

    2020-2021 Tesla Model 3: Swapped Camera Terminals Impair Collision Detection

    Tesla recalls 2020-2021 Model 3 and 2021 Model Y vehicles due to incorrectly installed camera cable terminals that cause swapped camera views, impairing collision detection and automatic emergency braking.

    Product
    TESLA — 2021 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V271000·2022-09-04

    2021 Porsche Cayenne recalled for rear axle suspension defect

    Porsche is recalling certain 2021 Cayenne models because lock nuts on the rear axle may break due to stress corrosion, potentially causing loss of control and crash risk.

    Product
    PORSCHE — 2021 PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V277000·2022-09-04

    2022 Kia Carnival fuel rail defect increases fire risk

    2022 Kia Carnival vehicles may have damaged fuel rail tubes that could leak fuel, increasing the risk of fire. Kia will inspect and replace affected fuel rails free of charge.

    Product
    KIA — 2022 KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V070000·2022-09-02

    2022 BMW X4 and Related Models Transmission Rollaway Risk Recall

    BMW is recalling certain 2022 330i, 530i, X3, and X4 vehicles because the transmission mechatronics unit may not have been properly assembled, potentially causing an internal leak that could lead to vehicle rollaway and crash risk.

    Product
    BMW — 2022 BMW X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22215·2022-09-01

    UPPAbaby RIDGE Jogging Strollers Recalled for Fingertip Amputation Hazard

    UPPAbaby is recalling about 14,400 All-Terrain RIDGE jogging strollers because openings in the rear disc brakes can catch and amputate a child's fingertip. One injury has been reported.

    Product
    UPPAbaby All-Terrain RIDGE Jogging Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22214·2022-09-01

    TJX Recalls Novogratz Outdoor Metal Hanging Chairs Due to Fall Hazard

    TJX Companies is recalling about 5,000 Novogratz outdoor metal hanging chairs sold nationwide. These chairs can tip or fall while occupied, or the supporting hooks or chains can break, causing 16 reported injuries including bruises and a mild concussion.

    Product
    Novogratz brand Outdoor Metal Hanging Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22769·2022-09-01

    Otter MOMO Children's Sandals Recalled for Excess Lead Content

    Kolan LLC is recalling about 100 Otter MOMO children's sandals sold on Amazon.com from March through April 2022 because the inner layer exceeds federal lead content limits. Lead can be toxic if ingested by young children.

    Product
    Otter MOMO Children's Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V022000·2022-09-01

    2021 Dutchmen Voltage recreational trailers recalled for mislabeled tire pressure

    Keystone RV Company is recalling 2021 Dutchmen Voltage trailers because the Federal Identification Tag incorrectly lists tire pressure as 95 PSI instead of 110 PSI, which could cause underinflated tires and increase crash risk.

    Product
    DUTCHMEN — 2021 DUTCHMEN VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide