The Recall Desk

State

Indiana product recalls

72,969 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,556
Critical
1,903
Severe
2,136
Most recent
2026-09-16

Of the 9,556 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 9,556 recalls whose distribution notice names Indiana specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6126–6150 of 82525

  • ModerateFDA (Food)·H-0380-2025·2025-08-06

    Organic Pure Stevia bottles actually contain mislabeled monk fruit powder

    Organic Pure Stevia, 1 oz, is being recalled because the product is monk fruit powder but the bottle was mislabeled as Organic Pure Stevia. 78 bottles are affected.

    Product
    Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Product is packaged in a plastic bottle with white cap. Ingredient: Organic Stevia Extract. Sprinkle a pinch for the perfect sweetness. Suggested Use: 1/64 tsp tastes as sweet as 1 tsp of sugar. Distributed by: NuNaturals, I
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2219-2025·2025-08-06

    ASPIRE Cristalle mammography systems shipped with unapproved slabbing software enabled

    ASPIRE Cristalle Mammography Systems with the Digital Breast Tomosynthesis option are being recalled because devices had an unapproved slabbing software function enabled for use. 293 units affected.

    Product
    ASPRIRE Cristalle Mammography System (cleared under K212873) installed with the ASPIRE Cristalle Digital Breast Tomosynthesis (DBT) Option (approved under P160031).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2196-2025·2025-08-06

    IontoPatch STAT nonwoven pads do not absorb the saline solution

    IontoPatch STAT On-the-Go Patch Therapy is being recalled because the nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with it. 80,928 units affected.

    Product
    IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2172-2025·2025-08-06

    Sterilizable Drill Stop Kits were shipped containing incorrect components

    The Drill Stop Kit, a version of the Mini Sterilizable Tray used to store, sterilize and verify drill stop length, is being recalled because it contains incorrect components. 45 kits affected.

    Product
    The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop length, and facilitate the mounting/removal of the Drill Stops. The Drill Stop Kit includes the Release Bracket, which is used for mounting and removing Drill Stops
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2197-2025·2025-08-06

    IontoPatch 80 nonwoven pads do not absorb the saline solution

    IontoPatch 80 On-the-Go Patch Therapy is being recalled because the nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with it. 63,936 units affected.

    Product
    IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2192-2025·2025-08-06

    Phasor neurosurgical drills may have a reverse battery orientation

    The Phasor Drill, used in neurosurgical procedures, is being recalled because it may have a reverse battery orientation, which may increase surgical time. 1,064 units are affected.

    Product
    Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-2195-2025·2025-08-06

    LYFO-DISK M. canis single packs may fail to recover the organism

    LYFO-DISK M. canis preparations, REF 0894L, are being recalled because they may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.

    Product
    LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V501000·2025-08-05

    2024–2026 International LT and 2025 RH Trucks Service Brake Defect

    International Motors is recalling certain 2024–2026 LT and 2025 RH trucks because the Hill Start Assist exhaust port may clog, preventing brake release and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E049000·2025-08-05

    Holley Recalls 140 GPH Electric Fuel Pumps Due to Methanol Incompatibility

    Holley Performance Products is recalling 140 GPH BLACK electric fuel pumps because they may not be compatible with methanol fuel, which can cause leaks and fire risks.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V499000·2025-08-04

    2024-2025 Winnebago Ekko RV Tire Valve Extension Defect Recall

    Winnebago is recalling certain 2024-2025 Ekko recreational vehicles due to damaged tire valve extensions that can cause air loss in the inner tire and overload the outer tire, creating a crash risk. Dealers will replace the extensions free of charge.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E048000·2025-08-01

    Bendix Recalls Knorr-Bresme Brake Chambers for Fire Risk

    Bendix is recalling specific Knorr-Bresme brake chambers for buses due to improper manufacturing that can cause air leaks and increase fire risk.

    Product
    PARKING BRAKE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25415·2025-07-31

    KidKraft play kitchen hooks caused a toddler's fatal strangulation in Oregon

    KidKraft Farm to Table play kitchens are being recalled because clothing can catch on the accessory hooks. A 23-month-old child died from strangulation and asphyxia in February 2023.

    Product
    KidKraft Farm to Table Model Play Kitchen
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25412·2025-07-31

    Cosco two-step kitchen stepper safety bars can detach or break

    The Cosco 2-Step Kitchen Stepper is being recalled because the safety bar can detach or break while in use. Thirty-four reports include two incidents resulting in head injuries.

    Product
    Cosco 2-Step Kitchen Stepper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25420·2025-07-31

    IKEA VÄRDEFULL garlic presses can shed small metal pieces

    IKEA 365+ VÄRDEFULL garlic presses are being recalled because small metal pieces can detach, posing laceration and ingestion hazards. Three lacerations have been reported globally.

    Product
    IKEA 365+ VÄRDEFULL garlic presses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25413·2025-07-31

    Tegu magnetic floating stacker toys can shed high-powered magnets

    Tegu Magnetic Floating Stackers are being recalled because magnets can loosen and detach, violating the mandatory standard for toy magnets. Thirty-one reports of magnets separating have been received.

    Product
    Magnetic Floating Stackers toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V498000·2025-07-31

    Storyteller Overland Recalls 2023 Mode LT RVs Due to Shore Power Fire Risk

    Storyteller Overland is recalling 2023 Mode LT recreational vehicles because improperly tightened shore power inlets may overheat and cause a fire. Dealers will replace the inlets free of charge.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND MODE LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25416·2025-07-31

    RIDGID brushless framing nailers can discharge a nail from the trigger alone

    RIDGID 18Volt Brushless 21-Degree and 30-Degree Framing Nailers are being recalled because the dual action engagement system can malfunction and involuntarily discharge a nail. About 64,000 units affected.

    Product
    RIDGID 18Volt Brushless 21-Degree Framing Nailers and RIDGID 18Volt Brushless 30-Degree Framing Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25414·2025-07-31

    Leatherman Charge Plus multi-tool knife blades do not fully fold in

    Leatherman Charge Plus and Charge Plus TTi multi-tools are being recalled because the tip of the knife blade does not fully fold into the handle, posing a laceration hazard. About 17,000 units affected.

    Product
    Leatherman Charge Plus and Charge Plus TTi Multi-Tools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V496000·2025-07-31

    Premier Trailer Recalls 2024 Reel and Pole Trailers Due to Brake Oil Leak

    Premier Trailer Solutions is recalling 2024 Reel and Pole trailers because improperly installed oil seals may leak oil onto the brake system, reducing braking ability.

    Product
    PREMIER TRALER — PREMIER TRALER REEL TRAILER, POLE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2025·2025-07-30

    SIGNA PET/MR gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA PET/MR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2025·2025-07-30

    Nellcor bedside SpO2 monitor alarms may not be heard or recognized

    The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.

    Product
    Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN
    Category
    Medical Device
    Distribution
    Distributed nationwide