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.

16051–16075 of 20364

  • HighFDA (Devices)·Z-1507-2022·2022-08-17

    Haiou Needle Retractable Safety Syringe recalls due to needle detachment risk

    Approximately 7,218,000 Haiou Needle Retractable Safety Syringes are being recalled due to needle detachment and retracting mechanism failures that increase needlestick injury risk. The affected product was distributed in California.

    Product
    Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 (0.6x25mm). 200pcs/Box Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-23G25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1319-2022·2022-08-17

    FDA Recalls Miralax Osmotic Laxative Powder for Storage Deviations

    The FDA recalled 67 bottles of Miralax laxative powder due to storage conditions that violated drug label specifications. The precautionary recall is due to potential product quality concerns from improper storage conditions.

    Product
    MIRALAX — MIRALAX (POLYETHYLENE GLYCOL 3350)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1316-2022·2022-08-17

    Eye Drops Recalled for Improper Storage Outside Specifications

    SYSTANE BALANCE lubricant eye drops (12 boxes, nationwide) are being recalled because they were stored outside the manufacturer's label specifications. The FDA classified this as a Class II recall.

    Product
    SYSTANE BALANCE — SYSTANE BALANCE (PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1325-2022·2022-08-17

    Racepinephrine Inhalation Solution Recalled for Improper Storage Conditions

    Mckesson Medical-Surgical is recalling S2 Racepinephrine Inhalation Solution due to storage that deviated from label specifications. This Class II recall affects 23 cartons distributed nationwide.

    Product
    S2 — S2 (RACEPINEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1322-2022·2022-08-17

    FDA Recalls A&D Original Ointment due to improper storage conditions

    A&D Original Ointment 16 oz jars are being recalled nationwide because products were stored outside manufacturer specifications. The recall affects all NDC 11523-0096-3 units distributed in the USA.

    Product
    A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC 11523-0096-3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1314-2022·2022-08-17

    FDA Recalls SYSTANE Lubricant Eye Drops Due to Improper Storage

    McKesson Medical-Surgical Inc. is recalling 47 bottles of SYSTANE Lubricant Eye Drops nationwide. The products were stored outside label specifications, violating manufacturing practices.

    Product
    SYSTANE LUBRICANT — SYSTANE LUBRICANT (POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1329-2022·2022-08-17

    Lamotrigine Tablets Recalled for Label Strength Error

    AVKARE Inc. is recalling 8,328 bottles of Lamotrigine Tablets, USP 100 mg nationwide due to a labeling error in the declared strength.

    Product
    LAMOTRIGINE — LAMOTRIGINE (LAMOTRIGINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1321-2022·2022-08-17

    FDA Recalls Pataday Eye Allergy Drops Due to Storage Deviations

    Mckesson Medical-Surgical is recalling Pataday Once Daily Relief eye drops nationwide because the products were stored outside label specifications. No illnesses have been reported.

    Product
    PATADAY ONCE DAILY RELIEF — PATADAY ONCE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1305-2022·2022-08-17

    Prescription Drug Recall: Telmisartan-Hydrochlorothiazide Tablets Due to Defective Packaging

    Glenmark Pharmaceuticals recalls 72,288 units of Telmisartan-Hydrochlorothiazide 80/25 mg tablets nationwide due to defective blister packaging that is difficult to open and causes tablets to break.

    Product
    TELMISARTAN AND HYDROCHLOROTHIAZIDE — TELMISARTAN AND HYDROCHLOROTHIAZIDE (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1323-2022·2022-08-17

    FDA Recalls Dakin's Solution Due to Storage Condition Deviations

    McKesson Medical-Surgical recalled 113 bottles of Dakin's Solution (sodium hypochlorite) nationwide due to improper storage outside label specifications. Products may have compromised stability.

    Product
    DAKINS QUARTER — DAKINS QUARTER (SODIUM HYPOCHLORITE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1318-2022·2022-08-17

    Earwax Removal Aid Debrox Recalled Nationwide for Improper Storage Conditions

    Debrox earwax removal aid is recalled nationwide because 131 boxes of the product were stored outside label-specified conditions. Consumers should discontinue use and consult a healthcare provider if needed.

    Product
    DEBROX — DEBROX (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1324-2022·2022-08-17

    Asthmanefrin Racephinephrine Inhalation Solution Recalled Due to Improper Storage

    Asthmanefrin Racephinephrine Inhalation Solution is being recalled because batches were stored outside the conditions specified on the drug label. The recall affects products distributed nationwide.

    Product
    Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of intermittent asthma, Preservative Free, Sterile, For Oral Inhalation Only, 30 vials per box, Nephron Pharmaceuticals Corporation, NDC 0487-2784-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1306-2022·2022-08-17

    Glenmark Pharmaceuticals Recalls Telmisartan/Hydrochlorothiazide Due to Defective Blister Packs

    Glenmark Pharmaceuticals Inc., USA is recalling specific lots of Telmisartan and Hydrochlorothiazide tablets due to complaints of defective blister packs that are difficult to open and cause tablets to break during removal.

    Product
    TELMISARTAN AND HYDROCHLOROTHIAZIDE — TELMISARTAN AND HYDROCHLOROTHIAZIDE (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1312-2022·2022-08-17

    Bisacodyl suppositories recalled nationwide due to improper storage

    McKesson Medical-Surgical is recalling Bisacodyl suppositories stored outside label specifications. The FDA Class II recall affects 45 boxes distributed nationwide.

    Product
    BISACODYL — BISACODYL (BISACODYL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·22200·2022-08-15

    4moms MamaRoo and RockaRoo Baby Swings and Rockers Strangulation Hazard

    4moms is recalling over 2 million MamaRoo baby swings and 220,000 RockaRoo rockers because dangling restraint straps pose a strangulation hazard to crawling infants. One death has been reported.

    Product
    4moms MamaRoo Baby Swing, versions 1.0 through 4.0 and RockaRoo Baby Rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V906000·2022-08-12

    2023 KIA Forte front left steering knuckle may crack

    Kia is recalling certain 2023 Forte vehicles due to a manufacturing error that may cause the front left steering knuckle to crack, resulting in loss of steering control and increased crash risk.

    Product
    KIA — 2023 KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V908000·2022-08-12

    2023 McLaren Artura recalled for fuel pipe defect increasing fire risk

    McLaren is recalling 164 2023 Artura vehicles because high-pressure fuel pipe nuts may loosen, causing fuel leaks that could lead to fires. Dealers will replace the fuel pipes at no cost.

    Product
    MCLAREN — 2023 MCLAREN ARTURA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V909000·2022-08-12

    School buses recalled for incorrectly tightened rear axle fasteners

    Navistar is recalling certain 2023-2024 IC BUS school buses due to fasteners on the rear axle that may have been tightened incorrectly. This can allow the rear axle to shift, reducing vehicle control and increasing crash risk.

    Product
    IC BUS — 2023 IC BUS EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V997000·2022-08-12

    2022 Entegra Vision Motorhomes Recalled for Melting Wiring Harness

    Jayco is recalling certain 2022 Entegra Vision motorhomes because the main chassis wiring harness may be positioned too close to the exhaust manifold, causing the wiring to melt. This can lead to vehicle stall and increased crash risk.

    Product
    ENTEGRA — 2022 ENTEGRA VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V907000·2022-08-12

    Subaru Ascent 2019–2022 Recall for Electrical Fire Risk

    Subaru is recalling 2019–2022 Ascent vehicles due to an improperly fastened ground bolt on the PTC heater that could melt and cause an electrical fire.

    Product
    SUBARU — 2019 SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V904000·2022-08-12

    2019-2022 RAM Pickup Trucks Recalled for Defective Tailgate Latch

    Chrysler is recalling 2019-2022 RAM 1500, 2500, and 3500 pickup trucks because the tailgate may not latch properly due to misaligned strikers. An unintended tailgate opening while driving could result in cargo loss and increased crash risk.

    Product
    RAM — 2022 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide