The Recall Desk

State

Idaho product recalls

20,371 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.

16676–16700 of 20371

  • SevereFDA (Food)·F-1239-2022·2022-06-15

    Chewing gum recalled nationwide for potential Salmonella contamination

    Elite Must Blueberry Sugar-Free Chewing Gum is recalled nationwide due to potential Salmonella contamination in all lots. Consumers should not consume this product.

    Product
    ELITE MUST BLUEBERRY FLAVORED SUGAR FREE CHEWING GUM UPC:815871013123 NET WT. .99oz (28 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1237-2022·2022-06-15

    Elite Bittersweet Chocolate Coins Recalled for Potential Salmonella Contamination

    Elite Confectionery LTD is recalling Elite Bittersweet Chocolate Coins nationwide due to potential Salmonella contamination. All lots with UPC 746132001255 are affected and should not be consumed.

    Product
    ELITE BITTERSWEET CHOCOLATE COINS UPC:746132001255 NET WT. .53oz (15 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1206-2022·2022-06-15

    Elite Mini Pesek Zman Classic Candy Recalled Nationwide for Salmonella Risk

    Elite Mini Pesek Zman Classic confectionery has been recalled nationwide due to potential Salmonella contamination. All lot numbers are affected.

    Product
    ELITE MINI PESEK ZMAN CLASSIC UPC: 815871015233 NET WT. 14.11 (400 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1207-2022·2022-06-15

    HeartWare HVAD Pump Implant Kit recalled for welding defect risk

    Medtronic is recalling HeartWare HVAD Pump Implant Kit units due to a welding defect in the center post cap that can lead to pump malfunction and affect blood flow.

    Product
    HeartWare HVAD Pump Implant Kit, a) Model Number 1104JP, b) Model Number MCS1705PU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1250-2022·2022-06-15

    Elite Bazooka Grape Gum Recalled for Potential Salmonella Contamination

    Elite Bazooka Grape Flavored Gum is being recalled nationwide due to potential Salmonella contamination. All lots are affected.

    Product
    ELITE BAZOOKA GRAPE FLAVORED GUM UPC:815871010467 NET WT. 0.99 (28 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1185-2022·2022-06-15

    Elite Aerated Milk Chocolate recalled nationwide for potential Salmonella

    Elite Confectionery Ltd is recalling all lots of Elite Aerated Milk Chocolate (3.17 oz, UPC 815871015431) distributed nationwide due to potential Salmonella contamination.

    Product
    ELITE AERATED MILK CHOCOLATE UPC:815871015431 Net Wt. 3.17 oz (90 g). Red packaging
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1228-2022·2022-06-15

    Elite Shtix With Milk Cream Candy Recalled for Salmonella Contamination Risk

    Elite Confectionery is recalling Elite Shtix candy nationwide due to potential Salmonella contamination. Consumers should not consume the product.

    Product
    ELITE SHTIX WITH MILK CREAM UPC:815871011037 & 815871011822 NET WT. 3.45oz (98 g). Shtix, blue label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1034-2022·2022-06-15

    FDA Recalls BSS Sterile Irrigating Solution for Manufacturing Temperature Deviations

    McKesson Medical-Surgical is recalling BSS sterile irrigating solution nationwide due to cGMP deviations involving temperature abuse during manufacturing. The recall affects prescription-only ophthalmic solutions.

    Product
    BSS — BSS (BALANCED SALT SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1037-2022·2022-06-15

    Meclizine Hydrochloride Tablets Recalled for Manufacturing Temperature Control Deviations

    Mckesson Medical-Surgical is recalling Meclizine Hydrochloride 25mg tablets nationwide due to manufacturing deviations involving improper temperature control. The FDA classified this as a Class II recall.

    Product
    MECLIZINE HYDROCHLORIDE — MECLIZINE HYDROCHLORIDE (MECLIZINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1004-2022·2022-06-15

    Lidocaine Patch 5% Recalled for Temperature Exposure During Distribution

    McKesson Medical-Surgical is recalling Lidocaine Patch 5% due to temperature abuse during storage and distribution. Affected patches may not function properly. Patients should consult their healthcare provider.

    Product
    Lidocaine Patch, 5%, 30-count box, Rx only, Manufacturer: Rhodes Pharmaceuticals, NDC 42858-0118-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1254-2022·2022-06-15

    MedMinder Medication Dispenser Emergency Alert Function No Longer Operational

    MedMinder Medication Dispensers will no longer connect to the emergency alert system for all models. The device's emergency communication capability has been discontinued for approximately 2,701 units nationwide.

    Product
    MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to communicate with emergency call center.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1035-2022·2022-06-15

    Ophthalmic Drug Isopto Atropine Recalled Due to Manufacturing Temperature Deviation

    McKesson Medical-Surgical is recalling 13 bottles of Isopto Atropine 1% ophthalmic solution due to temperature-abuse violations of manufacturing standards that may have affected product sterility.

    Product
    ISOPTO ATROPINE — ISOPTO ATROPINE (ATROPINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0998-2022·2022-06-15

    Bupivacaine Hydrochloride Injection Recalled for Temperature Storage Deviations

    McKesson Medical-Surgical is recalling Bupivacaine Hydrochloride Injection due to temperature abuse during storage that may have compromised product sterility. The recall affects 224 cartons distributed nationwide.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1029-2022·2022-06-15

    Ciprofloxacin eye drops recalled due to manufacturing temperature deviations

    McKesson is recalling Ciprofloxacin Ophthalmic Solution 0.3% nationwide due to temperature deviations during manufacturing. The FDA classifies this as a Class II recall.

    Product
    Ciprofloxacin Ophthalmic Solution 0.3%, 10 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc., NDC 61314-0656-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1025-2022·2022-06-15

    Amoxicillin capsules recalled due to temperature exposure during manufacturing

    McKesson Medical-Surgical is recalling Amoxicillin 500mg capsules distributed nationwide due to temperature abuse during manufacturing that may compromise product potency and effectiveness.

    Product
    AMOXICILLIN — AMOXICILLIN (AMOXICILLIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0986-2022·2022-06-15

    FDA Recalls Ethanol Injection Vials Due to Sterility Concerns

    US Specialty Formulations is recalling 781 vials of Ethanol for Injection 95% due to lack of assurance of sterility. The product was distributed nationwide to medical facilities and physician offices.

    Product
    Ethanol for Injection 95%, 67 mL Multi-Dose vial, Rx only, US Specialty Formulations, 1403 South Albert Street, Allentown, PA 18103, PN: 69389-06229
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1000-2022·2022-06-15

    Bupivacaine HCl Injection Recalled Due to Temperature Abuse Manufacturing Defect

    Bupivacaine HCl Injection multi-dose vials are being recalled due to temperature abuse during manufacturing. The product was distributed nationwide. Patients should consult their healthcare provider for alternative treatments.

    Product
    Bupivacaine HCl Injection, Multi dose vial, 0.25%, 50 mL/2.5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0249-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1103-2022·2022-06-15

    Ondansetron Tablets Recalled for Temperature Exposure During Storage

    McKesson is recalling Ondansetron Hydrochloride 8 mg tablets distributed nationwide due to temperature abuse during storage that may affect medication stability. Patients should contact their pharmacy or doctor.

    Product
    ONDANSETRON HYDROCHLORIDE — ONDANSETRON HYDROCHLORIDE (ONDANSETRON HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1256-2022·2022-06-15

    Reliance Synergy Washer/Disinfector fire hazard due to electrical contactor malfunction

    Steris Corporation is recalling Reliance Synergy Washer/Disinfector units due to a malfunctioning electrical contactor that can cause heating elements to overheat, creating a fire risk. Affected units may generate smoke and fire in the drying chamber.

    Product
    Reliance Synergy Washer/Disinfector
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1245-2022·2022-06-15

    Siemens Artis icono Angiography Systems: Risk of Electric Shock from Grounding Failure

    Siemens is recalling 51 Artis icono biplane angiography systems due to a potential grounding failure that could allow electric shock if someone contacts metallic parts during use.

    Product
    Artis icono biplane -angiography systems developed for single and biplane diagnostic imaging and interventional procedures SMN: 11327600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1071-2022·2022-06-15

    MethyLPREDNISolone Acetate Injectable Suspension Recall Due to Temperature Abuse

    McKesson Medical-Surgical is recalling MethyLPREDNISolone Acetate Injectable Suspension due to temperature abuse during storage that may compromise sterility and efficacy. The recall affects 65 vials distributed nationwide.

    Product
    MethyLPREDNISolone Acetate Injectable Suspension, USP, 200mg/5mL (40 mg/mL), 5 mL multi-dose vial, Rx only, MFG: Teva Pharma USA, NDC 0703-0043-01
    Category
    Drug
    Distribution
    Distributed nationwide