The Recall Desk

State

Idaho product recalls

20,083 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.

7026–7050 of 20083

  • ModerateFDA (Drugs)·D-0046-2025·2024-11-20

    Perio Maintenance Rinse Recalled for Subpotent Stannous Fluoride Concentration

    Keystone Industries is recalling Perio Maintenance Rinse due to subpotency—the stannous fluoride concentration is below specifications. Affected lots were distributed nationwide.

    Product
    Perio Maintenance Rinse 0.63% Stannous Fluoride Concentrated Solution, Rx Only, Net Wt. 10 oz. (283.5 g) pumps, Mint flavor, Manufactured by: Keystone Industries, 480 S. Democrat Rd., Gibbstown, NJ 08027, NDC 68400-202-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0460-2025·2024-11-20

    FDA Recalls MEERA CL Mobile Operating Tables for Unintended Movement Stops

    Getinge Usa Sales Inc is recalling 112 MEERA CL mobile operating tables because error code 50037 may cause the table to stop moving unexpectedly when controlled via IR hand control, resulting in procedural delays.

    Product
    MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 710001B0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0363-2025·2024-11-20

    Karl Storz Irrigation Tubing Recalled for Unapproved Label Use

    Karl Storz Endoscopy is recalling Irrigation Tubing for the Endomat Select UP210 because its label claims an intended use that the FDA has not approved for U.S. distribution.

    Product
    Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0350-2025·2024-11-20

    Medline arthroscopy surgical kits recalled for incomplete packaging seal

    Medline Industries is recalling 80 arthroscopy surgical convenience kits due to incomplete packaging seals. The affected lot numbers are 24GBI464 and 24HBO800.

    Product
    ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0045-2025·2024-11-20

    Hydralazine Tablets Recalled Due to Failed Impurities and Degradation Testing

    Hydralazine HCl Tablets 25mg are recalled nationwide due to failed impurities and degradation specifications. The recall affects approximately 25,814 tablets distributed by Avet Pharmaceuticals and MAJOR Pharmaceuticals.

    Product
    Hydralazine HCl Tablets, USP, 25mg, Rx only, 100 tablets per carton, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, Distributed by: MAJOR Pharmaceuticals, Livonia, MI, 48152, USA, NDC 0904-6441-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0043-2025·2024-11-20

    Lanthanum Carbonate 1000mg Chewable Tablets Recalled for Broken and Crushed Tablets

    Cipla USA is recalling Lanthanum Carbonate Chewable Tablets, 1000mg due to complaints of crushed and broken tablets. The recall affects 1,875 boxes distributed nationwide.

    Product
    Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·25046·2024-11-14

    Medical King adult bed rails recalled for entrapment and asphyxia hazard

    Medical King bed rails (about 222,000 units) are being recalled because they can trap users between the rail and mattress, posing asphyxiation risk. One death has been reported.

    Product
    Medical King Bed Assist Rail adult bed rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25043·2024-11-14

    woom Recalls Children's Bicycles Due to Crank Fractures and Fall Hazards

    woom Bike USA is recalling about 2,500 children's bicycles due to cranks that can break from fatigue fractures, causing riders to lose control and crash. One child was injured when this defect occurred.

    Product
    woom bicycles OFF 5, OFF AIR 5, OFF 6, OFF AIR 6, and ORIGINAL 6
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25042·2024-11-14

    Cultivar Planter Boxes Recalled Due to Breaking Frame and Injury Hazard

    Outdoor Essentials Cultivar Planter Boxes are being recalled due to breaking frames that pose an injury risk. The firm received 23 reports of frame breaks, including one consumer injury.

    Product
    Cultivar Planter Boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25045·2024-11-14

    DeNova Detect Combination Alarms Recalled for Failure to Alert to Carbon Monoxide

    New Cosmos USA recalls about 26,360 DeNova Detect combination natural gas and carbon monoxide alarms because they can enter sleep mode and fail to alert consumers to dangerous gas levels. No injuries have been reported.

    Product
    DeNova Detect Brand Combination Natural Gas and Carbon Monoxide Alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25041·2024-11-14

    Hallmark Christmas tree ornaments recalled due to mold growth

    Hallmark is recalling about 11,100 Cad Bane Christmas ornaments because mold grew on them when the paint did not fully dry before packaging. The mold poses a respiratory risk. No injuries have been reported.

    Product
    Hallmark Keepsake Christmas Tree Ornaments featuring the Cad Bane character from Star Wars: The Book of Boba Fett
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25040·2024-11-14

    Petidoux Children's Pajamas Recalled for Burn Hazard from Flammability Violation

    Petidoux is recalling about 620 Celebration Girl's Summer Pajama Sets due to a violation of federal flammability regulations for children's sleepwear. The pajamas pose a risk of burn injuries to children.

    Product
    Celebration Girl's Summer Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0040-2025·2024-11-13

    Ascorbic Acid Injection Recalled Nationwide for Glass Contamination

    Staska Pharmaceuticals recalled ascorbic acid injectable solution due to glass contamination. The FDA classified the recall as Class I; 4,773 vials nationwide were affected.

    Product
    Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0286-2025·2024-11-13

    epoc BGEM BUN Test Cards recalled for sodium measurement bias

    Siemens recalled epoc BGEM BUN Test Cards for a negative sodium bias occurring approximately 2 months before expiration, with maximum observed bias of -10 mmol/L. No adverse events reported.

    Product
    epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System, SMN 10736515
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0106-2025·2024-11-13

    MyChai Chai Tea Concentrate Recalled for pH Control and Documentation Issues

    MyChai Chai Tea Concentrate Original is recalled nationwide. The FDA found pH levels above 4.1 and missing production records.

    Product
    MyChai Chai Tea Concentrate Original. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 year expiration from date of manufacture. Ingredients: Water, Sugar, Organic Black Tea, Organ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0041-2025·2024-11-13

    Generic Ibuprofen 800mg Recalled Due to Failed Impurity and Degradation Specifications

    Direct Rx is recalling 1,410 bottles of Ibuprofen 800mg tablets distributed nationwide due to failed impurity specifications discovered during 18-month stability testing.

    Product
    Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg, Packaged and Distributed by: DIRECT Rx, Dawsonville, GA 30534, Mfg By: Dr. Reddy's Laboratories LA, LLC, Shreveport, LA 71106, a) NDC 61919-0621-15 (15 count bottles), b) NDC 61919-0621-30 (30 cou
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0307-2025·2024-11-13

    DeRoyal Children's Surgical Pack Recalled for Smoke Pencil Malfunction

    DeRoyal is recalling certain lots of children's surgical procedure packs due to reports that the included Stryker smoke evacuation pencil may activate without manual input or remain active after buttons are released.

    Product
    DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0037-2025·2024-11-13

    Morphine Sulfate Extended-Release Tablets Recalled for Failed Impurities Specification

    Dr. Reddy's Laboratories is recalling Morphine Sulfate Extended-Release Tablets 30 mg (Lot FG13996) nationwide due to failed impurities and degradation specifications.

    Product
    Morphine Sulfate Extended-Release Tablets 30 mg, 100-count bottles, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-186-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0285-2025·2024-11-13

    Endoscopic Vessel Harvesting System Recalled for Assembly Defect

    Zimmer recalls the Venapax XL endoscopic vessel harvesting system due to assembly defects that may cause endoscope interference during surgery. A Gen 5 tail piece was incorrectly assembled to Gen 4 devices, affecting 432 units nationwide.

    Product
    Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. Item Number: VPX4000 (7273)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0098-2025·2024-11-13

    Hammond's Dark Chocolate Waffle Cones Recalled for Undeclared Milk Allergen

    Hammond's Candies is recalling Dark Chocolate Filled Mini Waffle Cones nationwide due to undeclared milk allergen. Consumers with milk allergies should not consume this product.

    Product
    Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number: FC23212; UPC 6 91355 90513 5. Label declares ***CONTAINS: WHEAT, SOY, TREE NUTS (COCONUT)***PACKAGED IN A FACILITY THAT PROCESSES EGG, MILK, MUSTARD, PEANUTS, SE
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0309-2025·2024-11-13

    DeRoyal Surgical Procedure Pack Smoke Evacuation Pencil Recalled

    DeRoyal is recalling surgical procedure pack products containing a Stryker SafeAir Smoke Evacuation Pencil that may activate without manual input or remain active after buttons are released. The malfunction poses a risk of injury during surgical procedures.

    Product
    DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0036-2025·2024-11-13

    Morphine Sulfate Extended-Release Tablets Recalled for Impurities and Degradation

    Dr. Reddy's Laboratories is recalling Morphine Sulfate Extended-Release Tablets 15 mg nationwide due to failed impurity and degradation specifications. Patients taking affected lots should contact their healthcare provider immediately.

    Product
    Morphine Sulfate Extended-Release Tablets 15 mg, 100-count per bottle, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-185-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0308-2025·2024-11-13

    DeRoyal Children's Orthopedic Tracepack Smoke Evacuation Pencil Malfunction Recall

    DeRoyal is recalling 384 units of Children's Orthopedic TracePacks containing a Stryker smoke evacuation pencil that may activate unexpectedly or fail to deactivate, posing a burn risk during surgery.

    Product
    DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK, 89-9349-06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0318-2025·2024-11-13

    GE Healthcare Centricity Viewer Security Vulnerability Could Allow Unauthorized Access

    GE Healthcare's Centricity Universal Viewer Zero Footprint medical imaging software contains a security vulnerability that could allow unauthorized access and patient data manipulation. Approximately 120 units are affected worldwide.

    Product
    GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083, GDZH-JINWAN-Centricity 2) 2089507-093, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02268286, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02030900, 1495-1-Centric
    Category
    Medical Device
    Distribution
    Distributed nationwide