The Recall Desk

State

Idaho product recalls

72,936 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total
3,517
Critical
364
Severe
1,023
Most recent
2026-09-06

Of the 3,517 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,023 (29%) are Severe.

Which agencies issued them

These figures cover only the 3,517 recalls whose distribution notice names Idaho specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2926–2950 of 76453

  • HighFDA (Devices)·Z-1479-2026·2026-03-11

    Olympus lithotripsy generator recalled over transducer recognition failure

    Olympus is recalling the ShockPulse-SE Lithotripsy System Generator after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.

    Product
    Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V136000·2026-03-11

    Volvo EX30 seat belt warning chime may not sound as intended

    Volvo is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles because the seat belt warning system may not activate the audible warning chime. This fails FMVSS 208.

    Product
    VOLVO — VOLVO EX30CC, EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1485-2026·2026-03-11

    Aesculap MINOP trocar shafts may be longer than specified

    Aesculap is recalling MINOP Trocar 150 mm with 6.0 mm working channel, model FF399R, because of the potential for the trocar shaft to be too long.

    Product
    Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1488-2026·2026-03-11

    Olympus single use biopsy valve may shed rubber fragments during use

    Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-210, because of the potential for rubber fragment detachment during use.

    Product
    Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1478-2026·2026-03-11

    Olympus lithotripsy single use probes recalled over generator recognition failure

    Olympus is recalling ShockPulse-SE Lithotripsy System single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.

    Product
    Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0377-2026·2026-03-11

    Instant hand sanitizing wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Children's Healthcare of Atlanta Instant Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    Children's Healthcare of Atlanta, Instant Hand Sanitizing Wipe(Benzalkonium Chloride 0.13%), 1000 per case, Made in USA for Food Service Resources, Flowery Branch, GA 30542, NDC 0924-7130-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0362-2026·2026-03-11

    Bulk BZK antiseptic towelette brands recalled over manufacturing practice deviations

    Acme United Corporation is recalling BZK Antiseptic Towelettes sold under the Piedmont, Touchpoint, Wellstar Cobb and FSR names over current good manufacturing practice deviations.

    Product
    1) BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) 5"x7" Piedmont Sanitizing Hand Wipes, 1,000 ea Bulk, Made in USA for: Food Service Resources, Flowery Branch, GA 30542, NDC 0924-7130-00. 2) BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) 5" x 7" Touchpoint, 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0368-2026·2026-03-11

    WipesPlus alcohol free BZK wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes over current good manufacturing practice deviations.

    Product
    Wipes Plus, Hand Sanitizing Alcohol Free BZK Wipes (Benzalkonium Chloride 0.13%), Manufactured for: CFS Brands DBA WipesPlus, 4711 E. Heiner Rd. Oklahoma City, OK 73331, NDC 67151-333-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0379-2026·2026-03-11

    Semaglutide compounding ingredient lot recalled over incomplete validation before distribution

    Harbin Jixianglong Biotech is recalling a further lot of Semaglutide for prescription compounding because process validation and bacterial endotoxin method validation were not completed before distribution.

    Product
    Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04 Manufacturer: Harbin Jixianglong Biotech Co., Ltd., North of Baoan Road, East of Changqing Street,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0363-2026·2026-03-11

    Max Packaging antibacterial towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Max Packaging Antibacterial Towelettes over current good manufacturing practice deviations.

    Product
    Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0383-2026·2026-03-11

    Midodrine hydrochloride tablets recalled over inadequately sealed blister packaging

    The Harvard Drug Group is recalling one lot of Midodrine Hydrochloride Tablets 5 mg because of a defective container with inadequately sealed blister packaging.

    Product
    MIDODRINE HYDROCHLORIDE — MIDODRINE HYDROCHLORIDE (MIDODRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0372-2026·2026-03-11

    WipesPlus hand sanitizing wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67151-727-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0378-2026·2026-03-11

    Antimicrobial alcohol hand wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Antimicrobial Alcohol Hand Wipes containing 70% isopropyl alcohol over current good manufacturing practice deviations.

    Product
    Antimicrobial Alcohol Hand Wipe, Isopropyl Alcohol 70%, Manufactured for : Custom Packaging Co., Inc, Louisville, KY 4023, NDC 0924-251-00.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2026·2026-03-11

    Zone 2 lidocaine cream recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 2 4% Lidocaine Cream because the stability data does not support the labeled expiry date.

    Product
    MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1486-2026·2026-03-11

    Datascope CS100 balloon pump manual recalled for outdated battery specifications

    Datascope is recalling the CS100 IABP running software version Q.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.

    Product
    CS100 IABP. Software Version CS100 IABP Q.01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0365-2026·2026-03-11

    Medi-First antiseptic wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Medi-First Antiseptic Wipes over current good manufacturing practice deviations.

    Product
    MEDI-FIRST ANTISEPTIC WIPES — MEDI-FIRST ANTISEPTIC WIPES (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0370-2026·2026-03-11

    Med-Nap cleansing towelette bulk packs recalled over manufacturing deviations

    Acme United Corporation is recalling Med-Nap Cleansing Towelettes in bulk cases over current good manufacturing practice deviations.

    Product
    MED NAP CLEANSING TOWELETTE — MED NAP CLEANSING TOWELETTE (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0386-2026·2026-03-11

    Zone 1 lidocaine cream recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 1 4% Lidocaine Cream because the stability data does not support the labeled expiry date.

    Product
    MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0358-2026·2026-03-11

    First Aid Only BZK antiseptic wipes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY BZK ANTISEPTIC — FIRST AID ONLY BZK ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide