The Recall Desk

State

Indiana product recalls

72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7851–7875 of 82542

  • HighNHTSA·25V151000·2025-03-11

    Keystone travel trailer wiring lacks sufficient surge protection

    Keystone RV is recalling certain 2025 Kodiak, Colorado and Sunset travel trailers because the 7-way cord and 12-volt distribution box were wired with insufficient surge protection.

    Product
    KEYSTONE — KEYSTONE KODIAK, COLORADO, SUNSET TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V153000·2025-03-11

    Nissan Sentra driver seat frames may not be fully secured

    Nissan is recalling certain 2025 Sentra vehicles because the driver's seat frame may not be fully secured to the outer side of the seat track, failing FMVSS 207 and 210.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V150000·2025-03-07

    Mercedes-Benz Recalls 2023 EQE Models for Detaching Wheel Rim Inserts

    Mercedes-Benz is recalling 2023 EQE 350 4MATIC and EQE 350+ vehicles because wheel rim inserts may detach while driving, creating a crash hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ redundant EQE 350 4MATIC, EQE 350+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V149000·2025-03-07

    2025 Forest River Aurora Travel Trailers Electrical Fire Risk Recall

    Forest River is recalling certain 2025 Aurora ART26BHS travel trailers because the air conditioner electrical connector may have exposed wiring strands that can cause electrical arcing and fire.

    Product
    FOREST RIVER — FOREST RIVER AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25160·2025-03-06

    Nuby Stroller Fans recalled due to laceration injury hazard

    Nuby Stroller Fans are recalled because the housing allows children's fingers to contact the spinning blade, causing lacerations; six injuries have been reported. Consumers should stop using the product immediately and contact the manufacturer for a free replacement.

    Product
    Nuby Stroller Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25168·2025-03-06

    Children's Nightgowns and Robes Recalled for Flammability and Burn Hazard

    Marie-Chantal children's nightgowns, pajama sets and robes violate federal flammability standards for sleepwear, posing a risk of serious burn injuries. About 560 units sold nationwide from November 2021 through October 2024; consumers should stop use immediately.

    Product
    Marie-Chantal Children's Nightgowns, Pajama Sets and Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25170·2025-03-06

    Auto World Unassembled Slot Cars Recalled for Loose Magnet Ingestion Hazard

    About 55,000 Auto World Unassembled Deluxe Pit Kit Slot Cars are being recalled because loose magnets in unassembled kits pose an ingestion hazard to children. The products were sold nationwide from July 2023 to February 2024.

    Product
    Auto World Unassembled Deluxe Pit Kit Slot Cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25172·2025-03-06

    Love Our Home Crib Bumpers Recalled for Federal Ban Violation and Suffocation Risk

    Love Our Home braided crib bumpers sold on Shein.com violate the federal Safe Sleep for Babies Act and pose a suffocation hazard to infants. About 750 units were sold between March and November 2024.

    Product
    Love Our Home Braided Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25173·2025-03-06

    Taylor Water Technologies Recalls Phosphate Reagent Bottles Due to Chemical Burn Risk

    Taylor Water Technologies is recalling about 10,000 Phosphate Reagent #1 bottles sold with test kits. The sulfuric acid bottles lack required child-resistant packaging, posing a risk of severe chemical burns.

    Product
    Phosphate Reagent #1 Bottles sold within the Taylor Phosphate Test Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25167·2025-03-06

    BD Recon LT Avalanche Transceivers Recalled Due to Switch Corrosion

    BD Recon LT avalanche transceivers are recalled because the switch mechanism can corrode and fail, potentially preventing rescuers from locating avalanche victims. Six devices have malfunctioned; no injuries reported.

    Product
    BD Recon LT Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V146000·2025-03-06

    2024 Kawasaki Z500 and Ninja 500 Motorcycles Clutch Release Shaft

    Kawasaki is recalling certain 2024 Z500 and Ninja 500 motorcycles due to improper welding of the clutch release shaft, which can cause the clutch lever to break and disable the motorcycle, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA 500, Z500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V148000·2025-03-06

    Cadillac CT5 and related vehicles transmission lock-up recall

    General Motors is recalling certain 2019–2022 Cadillac and Chevrolet vehicles with 10-speed transmissions due to internal transmission damage that may cause wheel lock-up while driving.

    Product
    CHEVROLET — CHEVROLET, CADILLAC CAMARO, CT5, CT4, CT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V145000·2025-03-06

    Jayco Recalls 2024-2025 Motorhomes Due to Incorrect Federal Load Labels

    Jayco is recalling specific 2024 and 2025 motorhomes because incorrect Federal labels may allow the vehicles to be overloaded, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, ALANTE SE, REDHAWK SE, ODYSSEY SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V147000·2025-03-06

    2024 INEOS GRENADIER door latch assembly defect recall

    INEOS is recalling certain 2024 Grenadier vehicles because the door button mechanism may lack sufficient grease, preventing the door from fully latching. An unlatched door can open unexpectedly while driving, increasing injury risk.

    Product
    INEOS — INEOS GRENADIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0578-2025·2025-03-05

    Gerber Baby Teething Sticks Recalled Due to Choking Risk

    Nestlé-USA is recalling all lots of Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Strawberry Apple flavor following complaints of infant choking. The product was distributed across 42 states and Puerto Rico.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    46 states
  • SevereFDA (Food)·F-0579-2025·2025-03-05

    Gerber Baby Soothe 'n' Chew Teething Sticks Recalled for Choking Risk

    Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Banana flavor are recalled nationwide due to complaints of infant choking. All lots in both 1.59 oz and 3.2 oz packages are affected.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    46 states
  • SevereNHTSA·25V143000·2025-03-05

    Airstream Recalls Classic Travel Trailers Due to Fire Risk

    Airstream is recalling certain Classic travel trailers because the sofa footrest switch wiring may overheat, increasing the risk of a fire.

    Product
    AIRSTREAM — AIRSTREAM CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1223-2025·2025-03-05

    FDA Recalls Medial Tibia Plates for Intra-operative Screw Failure

    Tyber Medical is recalling A.L.P.S. mvX Medial Tibia Plates due to reports that the locking screw can pass through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770715121
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1216-2025·2025-03-05

    Anatomic lateral fibula plate locking screw failure during surgery

    Tyber Medical A.L.P.S. mvX anatomic lateral fibula plates (219 units nationwide) have a defect where the locking screw can pass through its locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate, 10-Hole, Right. Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770708102 Product Description:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1241-2025·2025-03-05

    GE Healthcare MRI system recalled for RF energy safety control failure

    GE Healthcare's Optima MR360 MRI systems may allow unsafe RF energy exposure if a scan resumes after power loss. The user interface can incorrectly enable scanning when tissue-heating levels exceed safe limits.

    Product
    Optima MR360, NMRI system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1247-2025·2025-03-05

    Leica Biosystems Cryostat CM1950 Firmware Update May Cause Tissue Loss

    A software issue in the Leica Biosystems CM1950 cryostat firmware update could result in loss of patient tissue. Serial numbers 12835 and 12854 are affected.

    Product
    Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog Number: 1491950C4US Software Version: firmware V3.01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1230-2025·2025-03-05

    BD Pyxis MedBank medication cabinets recalled for operating room contraindication labeling

    CareFusion is recalling BD Pyxis MedBank medication management cabinets due to inadequate labeling. A contraindication statement must be added to warn against use in procedure and operating rooms.

    Product
    139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS
    Category
    Medical Device
    Distribution
    Distributed nationwide