The Recall Desk

State

Indiana product recalls

72,936 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,555
Critical
1,903
Severe
2,136
Most recent
2026-09-09

Of the 9,555 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.

These figures cover only the 9,555 recalls whose distribution notice names Indiana specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3026–3050 of 82491

  • 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
  • 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-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-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-0380-2026·2026-03-11

    Semaglutide compounding ingredient recalled over incomplete process and endotoxin validation

    Harbin Jixianglong Biotech is recalling Semaglutide for prescription compounding use 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; e) 100g, NDC 84385-106-05Manufacturer: Harbin Jixianglong Biotech Co., Ltd., North of Baoan Road,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0359-2026·2026-03-11

    First Aid Only BZK antiseptic towelettes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY BZK ANTISEPTIC — FIRST AID ONLY BZK ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1487-2026·2026-03-11

    Datascope CS300 balloon pump manual recalled for outdated battery specifications

    Datascope is recalling the CS300 IABP running software version C.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.

    Product
    CS300 IABP. Software Version CS300 IABP C.01.
    Category
    Medical Device
    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-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-0367-2026·2026-03-11

    Med-Nap BZK antiseptic towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Med-Nap BZK Antiseptic Towelettes in bulk packs over current good manufacturing practice deviations.

    Product
    MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC — MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0364-2026·2026-03-11

    Savannah antibacterial towelettes recalled over manufacturing practice deviations

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

    Product
    Savannah Antibacterial Towelettes (Benzalkonium Chloride 0.13%), 1 towelette, 4 x 7, R&R Enterprise, NDC 59647-749-02
    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-0366-2026·2026-03-11

    Med-Nap BZK antiseptic towelettes recalled over manufacturing practice deviations

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

    Product
    MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC — MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0381-2026·2026-03-11

    Nilotinib capsules recalled after failing appearance tests at six months

    Cipla USA is recalling three lots of Nilotinib Capsules 150 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0382-2026·2026-03-11

    Nilotinib 200 mg capsules recalled after failing appearance tests

    Cipla USA is recalling one lot of Nilotinib Capsules 200 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V134000·2026-03-06

    Mercedes-Benz Recalls 2026 GLA 250 for Door Latch Defect

    Mercedes-Benz is recalling 2026 GLA 250 vehicles because an incorrectly installed bowden cable may prevent the door from opening from inside, potentially trapping occupants.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V135000·2026-03-06

    2026 Kia K4 vehicles recalled for defective rear seat belt anchor

    Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.

    Product
    KIA — KIA K4, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V128000·2026-03-05

    Toyota Highlander second-row seat backs may fail to lock

    Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V129000·2026-03-05

    GM heavy duty pickup fuel pump may cause an engine stall

    GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide