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.

16576–16600 of 20371

  • HighFDA (Drugs)·D-1145-2022·2022-06-22

    Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Concerns

    Sun Pharmaceutical is recalling 4,625 syringes of Medroxyprogesterone Acetate Injectable Suspension (Lot HAC1951A) due to lack of assurance of sterility. The affected medication was distributed nationwide.

    Product
    MEDROXYPROGESTERONE ACETATE — MEDROXYPROGESTERONE ACETATE (MEDROXYPROGESTERONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1129-2022·2022-06-22

    Homeopathic Colibacillinum Drug Recall Due to Manufacturing Deviations

    Washington Homeopathic Products recalls Colibacillinum homeopathic drug products due to manufacturing practice deviations. The recall involves 206 bottles distributed nationwide; the manufacturer voluntarily initiated it in May 2022.

    Product
    Colibacillinum, Potency: 12C, 14C, 15C, 18C, 20C, 30C, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1132-2022·2022-06-22

    Medorrhinum homeopathic drug recalled for manufacturing process deviations

    Washington Homeopathic Products recalled Medorrhinum liquid pellets nationwide due to deviations from manufacturing standards. The product was distributed in 49 glass amber bottles.

    Product
    Medorrhinum, Potency:12C, 30C, 200C, 1M, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1133-2022·2022-06-22

    Homeopathic Drug Morbillinum Recalled for Manufacturing Practice Deviations

    Washington Homeopathic Products is recalling Morbillinum in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.

    Product
    Morbillinum, Potency:7C, 8C, 9C, 10C 12C, 13C, 15C, 20C, 21C, 30C, 200 C,Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1136-2022·2022-06-22

    Pyrogenium Homeopathic Remedy Recalled for Manufacturing Process Violations

    Washington Homeopathic Products is recalling Pyrogenium homeopathic remedies in multiple potencies due to current Good Manufacturing Practice (cGMP) deviations. The firm initiated this voluntary recall affecting 6,782 bottles distributed nationwide.

    Product
    Pyrogenium, Potency: 15X, 16X, 17X, 19X, 21X, 22X, 25X, 30X, 1M, 200C, 30C, OTC, Liquid Pellets, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1159-2022·2022-06-22

    Artri King Reforzado con Ortiga Omega 3 Tablets Recalled as Unapproved Drug

    Walmart Inc is recalling Artri King Reforzado con Ortiga Omega 3 Tablets nationwide because the product was marketed as a drug without FDA approval. All lots are affected.

    Product
    Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1128-2022·2022-06-22

    Candida Parapsilosis homeopathic remedy recalled for manufacturing practice deviations

    Washington Homeopathic Products is recalling Candida Parapsilosis homeopathic remedies distributed nationwide due to manufacturing practice deviations. The recall affects 134 bottles under lot numbers 22315 and 26502.

    Product
    Candida Parapsilosis, Potency: 14X, 15X, 16X, 20X, 28X, 30X, 9C, 10C, 13C, 15C, 25C, 30C, 13X, 27X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1141-2022·2022-06-22

    Homeopathic Drug Recall: Vaccinotoxinum Products Due to Manufacturing Violations

    Washington Homeopathic Products is recalling Vaccinotoxinum homeopathic remedies (lot numbers 2512K and 20280) distributed nationwide due to cGMP manufacturing deviations. The voluntary recall was initiated by the firm in May 2022.

    Product
    Vaccinotoxinum, Potency: 32X, 11C, 30C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1127-2022·2022-06-22

    Homeopathic Drug Recall: Candida Albicans Remedy for Manufacturing Quality Issues

    Washington Homeopathic Products is recalling Candida Albicans homeopathic remedy due to manufacturing quality control violations. The voluntary recall affects 1,047 bottles distributed nationwide.

    Product
    Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C, 19C, 24C, 25C, 26C, 30C, 200C, 14X, 15X, 16X, 20X, 288X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1140-2022·2022-06-22

    Drug recall: Tuberculinum Bovinum due to manufacturing practice deviations

    Washington Homeopathic Products is recalling Tuberculinum Bovinum homeopathic remedy due to current good manufacturing practice deviations. No illnesses have been reported.

    Product
    Tuberculinum Bovinum, Potency: 12C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1134-2022·2022-06-22

    Homeopathic Drug Pertussinum Recalled Due to Manufacturing Deviations

    Washington Homeopathic Products is recalling Pertussinum in multiple potencies nationwide due to manufacturing practice deviations. Affected lot numbers are 18829, 20142, and 25410.

    Product
    Pertussinum, Potency: 19C, 30C, 200C, 1M, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1125-2022·2022-06-22

    Homeopathic Drug Anthracinum Recalled Over Manufacturing Compliance Deviations

    Washington Homeopathic Products is recalling Anthracinum liquid pellets due to manufacturing process deviations. The voluntary recall affects 219 bottles distributed nationwide.

    Product
    Anthracinum, Potency: 6C, 7C, 8C, 9C, 12C, 14C, 30C, 200C, 11X, 14X, 30X Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1138-2022·2022-06-22

    Syphilinum homeopathic drug recalled for manufacturing practice deviations

    Washington Homeopathic Products is recalling Syphilinum homeopathic products in multiple potencies due to current good manufacturing practice deviations. The affected products were distributed nationwide.

    Product
    Syphilinum, Potency: 9C, 30C, 200C, 10X, 12X, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1131-2022·2022-06-22

    Homeopathic drug Influenzinum recalled for manufacturing process deviations

    Washington Homeopathic Products is recalling Influenzinum in multiple potencies due to manufacturing process deviations. The recall affects approximately 6,400 units distributed nationwide.

    Product
    Influenzinum, Potency: 9X, 10X, 12X, 15X, 25X, 30X, 200C, 12C, 30C 1M, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1137-2022·2022-06-22

    Streptococcinum Homeopathic Drug Recalled Due to Manufacturing Deviations

    Washington Homeopathic Products is voluntarily recalling Streptococcinum homeopathic drug in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.

    Product
    Streptococcinum, Potency: 8C, 9C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1130-2022·2022-06-22

    Homeopathic Drug Diphtherinum Recalled for Manufacturing Practice Deviations

    Washington Homeopathic Products is recalling Diphtherinum homeopathic remedy (potencies 14C, 30C, 200C) distributed nationwide due to manufacturing practice deviations (cGMP violations). Affected lots: 20332, 20333.

    Product
    Diphtherinum, Potency: 14C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1158-2022·2022-06-22

    Artri Ajo King Tablets Recalled for Unapproved Drug Claims

    Walmart is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets nationwide. The product was marketed without FDA approval based on unapproved labeling claims.

    Product
    Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1148-2022·2022-06-22

    Premium Nature Hand Sanitizer Recalled for Subpotent Ethanol Content

    AMS Packaging is recalling Premium Nature Instant Hand Sanitizer nationwide because FDA analysis found some bottles contain less ethanol than labeled.

    Product
    Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML plastic bottles; Premium Nature, South Plainfield, NJ. UPC 819192028668
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1139-2022·2022-06-22

    Homeopathic Tuberculinum Drug Recalled for Manufacturing Practice Deviations

    Washington Homeopathic Products is recalling Tuberculinum homeopathic drug in multiple potencies due to manufacturing practice deviations. The voluntary recall affects product distributed nationwide.

    Product
    Tuberculinum, Potency: 1X, 12X, 24X, 30X, 1M, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·22163·2022-06-16

    Nest Swing Egg Chairs Recalled Due to Fall Hazard

    TJX is recalling approximately 30,600 Nest Swing Egg Chairs sold at Marshalls, T.J. Maxx, HomeGoods, and Homesense stores because the chairs can tip over or collapse when occupied, posing a fall hazard.

    Product
    Nest Swing Egg Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22168·2022-06-16

    WarmWave and Hunter Ceramic Tower Heaters Recalled for Fire and Burn Hazards

    Sienhua Group is recalling about 580,000 WarmWave and Hunter Oscillating Ceramic Tower Heaters because the cord and plug can overheat during use, posing fire and burn risks. The company has received eight reports of fires at the plug or cord and dozens of reports of overheating.

    Product
    WarmWave and Hunter Oscillating Ceramic Tower Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22159·2022-06-16

    Schneider Electric Electrical Panels Recalled for Fire and Burn Hazards

    Schneider Electric is recalling about 1.4 million Square D QO Plug-on-Neutral Load Centers because they can overheat, creating thermal burn and fire hazards. The company is contacting purchasers and installers to arrange free inspections and repairs.

    Product
    Square™ D QO™ Plug-on-Neutral Load Centers, also known as, Load Centers, Breaker Boxes, Electrical Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22164·2022-06-16

    Kroger Arthritis Pain Acetaminophen Recalled for Non-Child-Resistant Packaging

    Kroger-brand acetaminophen tablets in 225-count bottles lack required child-resistant packaging, posing a poisoning risk to young children if ingested. About 25,660 units were sold nationwide from December 2021 through March 2022.

    Product
    Kroger Arthritis Pain Acetaminophen, 225 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22162·2022-06-16

    Kroger Acetaminophen Recalled for Non-Child-Resistant Packaging

    Sun Pharmaceutical is recalling Kroger brand acetaminophen 650 mg extended-release caplets because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a risk of poisoning if swallowed by young children.

    Product
    Kroger Acetaminophen, 100 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22161·2022-06-16

    Walgreens Acetaminophen Bottles Recalled for Non-Compliant Packaging

    Aurohealth recalled Walgreens brand acetaminophen 500 mg bottles (150 count) because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a poisoning risk to young children.

    Product
    Walgreens Pain Reliever Acetaminophen, 150 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide