The Recall Desk

State

Idaho product recalls

20,187 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.

8726–8750 of 20187

  • HighFDA (Devices)·Z-2138-2024·2024-06-19

    EVD Catheter Sterile Packaging Defect Recall for Intracranial Drainage

    Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.

    Product
    CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2142-2024·2024-06-19

    VITROS Immunodiagnostic Calibrators Recalled for Potential Accuracy Bias

    Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.

    Product
    VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled Calibrator tube (1 per level: C1 - green, C2 - yellow, C3 - red).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2139-2024·2024-06-19

    Aeos Robotic Digital Microscope recalled for safety mechanism failure

    Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.

    Product
    Aeos Robotic Digital Microscope, Product Code: PV010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2032-2024·2024-06-19

    Streptococcal A Rapid Test Kits Recalled for Unauthorized At-Home Distribution

    Wondfo USA recalls Areta Strep A test kits (Lot E03920802) distributed for unauthorized at-home and over-the-counter use. The recall affects 75,000 units distributed nationwide.

    Product
    Streptococcal A rapid test kits, labeled as: Easy Healthcare Corporation, Areta Strep A Swab Test and EASY at Home Medical LLC, Areta One Step Strep A Swab Test, Part Number ARST-100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2143-2024·2024-06-19

    Darby Dental Prophylaxis Paste Mislabeled with Incorrect Part Number

    Young Dental Manufacturing is recalling 534 units of Darby Prophylaxis Paste with 1.23% Fluoride Ion (Lot 248607) due to incorrect part number labeling. The product was labeled as part number 045032 instead of the correct 040032.

    Product
    Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0550-2024·2024-06-19

    Asmanex (Mometasone Furoate) Recalled Due to Defective Container

    Organon LLC has voluntarily recalled 2,886 units of Asmanex inhalation powder nationwide due to defective containers.

    Product
    ASMANEX — ASMANEX (MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0552-2024·2024-06-19

    Asmanex Twisthaler inhalation powder recalled due to defective container

    Organon LLC is recalling Asmanex Twisthaler (mometasone furoate) inhalation powder nationwide due to defective containers. Affected lot #Y000085 expires April 25, 2025.

    Product
    Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 30 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-0114-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2132-2024·2024-06-19

    Medical device nerve block needles incorrectly labeled as DEHP-free

    Stimuplex A nerve block needles labeled as DEHP-free contain trace amounts of DEHP in the adhesive. B Braun is recalling approximately 1.78 million units distributed in the US and Canada.

    Product
    Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0551-2024·2024-06-19

    ASMANEX Inhalation Powder Recalled Due to Defective Container

    Organon LLC is recalling 2,551 units of ASMANEX Twisthaler mometasone furoate inhalation powder nationwide due to defective containers. Affected lot X024051 expires April 25, 2025.

    Product
    ASMANEX — ASMANEX (MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2037-2024·2024-06-19

    NEOMED Oral Syringes Recalled Over Missing Expiration Dates on Labels

    Avanos Medical is recalling NEOMED oral syringes because expiration dates were not printed on outer shipping labels, allowing expired units to reach customers.

    Product
    NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a.0.5mL Oral Syringe Orange NonSterile, Product Code BC-S05EO; b. 12mL Oral Syringe Orange NonSterile, Product Code BC-S12EO; c. 1mL Oral Syringe Orange NonSterile, Product Code BC-S1EO;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2030-2024·2024-06-19

    Strep A Rapid Test Kits Recalled for Unauthorized Distribution

    Wondfo USA is recalling approximately 1.2 million Preview Strep A rapid test kits (Part Numbers PRE-STA-25 and PRE-STA-A-10) that were distributed for at-home and direct-to-consumer use. The device is intended for professional channels only.

    Product
    Preview Strep A, Streptococcal A rapid test kits, Part Numbers: a) PRE-STA-25, b) PRE-STA-A-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2036-2024·2024-06-19

    NEOMED nonsterile pharmacy syringes recalled for missing expiration dates on labels

    Avanos Medical recalls NEOMED nonsterile pharmacy syringes because expiration dates were not printed on outer shipping labels, resulting in expired products being distributed.

    Product
    NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Blue NonSterile, Product Code BB-S05EO; b. 12mL Oral Syringe Blue NonSterile, Product Code BB-S12EO; c. 1mL Oral Syringe Blue NonSterile, Product Code BB-S1EO; d. 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2035-2024·2024-06-19

    NEOMED Pharmacy Syringes recalled due to missing expiration dates

    Avanos Medical is recalling NEOMED Pharmacy Syringes because expiration dates were not printed on the outer shipping labels. Approximately 37,476 cases of various syringe sizes were distributed worldwide.

    Product
    NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Amber NonSterile, Product Code BA-S05EO; b. 12mL Oral Syringe Amber NonSterile, Product Code BA-S12EO; c. 1mL Oral Syringe Amber NonSterile, Product Code BA-S1EO; d
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·24265·2024-06-13

    Magnetic Chess Games Recalled for High-Powered Magnet Ingestion Hazard

    About 2,600 magnetic chess games with 20 magnet pieces sold on Temu.com from December 2023 through February 2024 are recalled because the magnets violate federal toy magnet regulations and pose a serious ingestion hazard.

    Product
    1 Set Puzzle "Magnetic", "Magnetism", or "Magnetism Intelligence Strategy Game" Magnetic Battle Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24262·2024-06-13

    Southern Telecom Recalls Lomi Roll-On Waxing Kits for Fire and Shock Hazards

    Southern Telecom is recalling about 19,500 Lomi Roll-On Waxing Kits because the power cord can overheat and short circuit, creating fire, burn, and electrical shock hazards. Two consumers suffered burns and one incident of property damage has been reported.

    Product
    Lomi Roll-On Waxing Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24263·2024-06-13

    Nap Queen Sleep Victoria Hybrid Mattresses Recalled for Fire Hazard

    Adven Group is recalling approximately 117,200 Nap Queen Sleep Victoria Hybrid Mattresses sold nationwide from February 2020 through October 2023 because they violate federal flammability regulations, posing a fire hazard.

    Product
    Nap Queen Sleep Victoria Hybrid Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24261·2024-06-13

    Black Diamond Neve Strap Crampons Recalled Due to Fall Hazard

    Black Diamond Equipment is recalling Neve Strap Crampons and Accessory Kits because screws connecting the heel cup to the crampon can loosen, causing the heel cup to detach and creating a fall hazard. The firm has received three reports of incidents but no injuries have been reported.

    Product
    Neve Strap Crampons and Accessory Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24266·2024-06-13

    Beaumont Plus ST Bicycles with Disc Brakes Recalled for Brake Failure Risk

    Retrospec is recalling about 530 Beaumont Plus ST bicycles with disc brakes because the front brake rotor and pads can become misaligned, potentially causing brake failure and crashes. No injuries have been reported.

    Product
    Beaumont Plus ST Bikes with disc brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24264·2024-06-13

    Bambu Lab A1 3D Printers Recalled for Electric Shock and Fire Hazards

    Bambu Lab is recalling about 12,800 A1 3D printers sold between December 2023 and January 2024 due to damaged or bent heatbed cables that can short-circuit, spark, or burn through insulation, creating electric shock and fire risks. No injuries have been reported.

    Product
    Bambu Lab A1 3D printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24260·2024-06-13

    Daikin Air Conditioning and Heat Pump Units Recalled for Fire Hazard

    Daikin Comfort Technologies Manufacturing is recalling about 12,100 Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units due to incorrect electrical ratings on the serial plate that could lead to improper wiring and fire risk.

    Product
    Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1920-2024·2024-06-12

    Pediatric Patient Return Electrode Recalled for Reported Patient Burns

    Megadyne Medical Products is recalling its MEGA SOFT Pediatric Patient Return Electrode due to reports of patient burns during electrosurgical use. Approximately 1,270 units distributed worldwide are affected.

    Product
    MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long x 30.5cm Wide x 1.25cm. Electrosurgical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1880-2024·2024-06-12

    Arrow Ultra 8 Intra-Aortic Balloon Catheter Kit Recalled for Inflation Defect

    The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.

    Product
    Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit, a) REF IAB-05830-U; b) REF IAB-05840-U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1878-2024·2024-06-12

    Intra-Aortic Balloon Catheter Kit Recalled for Inflation and Structural Defects

    Arrow International is recalling intra-aortic balloon catheter kits due to potential inflation failure, catheter damage, and helium loss that could cause serious health consequences.

    Product
    Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1879-2024·2024-06-12

    Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled for Device Malfunction

    Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.

    Product
    Arrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840-U; c) REF IAB-06850-U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V858000·2024-06-12

    Fuel pump failure recall for 2013-2023 Honda and Acura vehicles

    Honda is recalling certain 2013-2023 Honda Accord, Civic, CR-V, HR-V, Odyssey, Pilot, Ridgeline and Acura ILX, MDX, RDX, RLX, TLX vehicles because the fuel pump inside the fuel tank may fail, potentially causing engine stall while driving and increasing crash risk.

    Product
    ACURA — 2020 ACURA RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide