The Recall Desk

State

Indiana product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9476–9500 of 82548

  • SevereCPSC·25038·2024-11-07

    Portable Lamps Recalled Due to Fire Hazard from Battery Overheating

    About 5,300 Tala Muse Portable Lamps are recalled due to fire hazard from battery overheating. One incident caused property damage; consumers should stop using the lamps and contact Tala for a free replacement bulb.

    Product
    Tala Muse Portable Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25036·2024-11-07

    Smart Electric Space Heaters Recalled for Fire and Burn Hazards

    GoveeLife and Govee smart electric space heaters can overheat and pose fire and burn hazards due to non-compliance with UL 1278 safety standards. About 512,500 units are affected.

    Product
    GoveeLife and Govee Smart Electric Space Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V840000·2024-11-07

    Land Rover Recalls 2014-2016 Range Rovers for Suspension Defect

    Jaguar Land Rover is recalling 2014-2016 Range Rovers because a front suspension part may crack, risking loss of vehicle control.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V841000·2024-11-07

    Micro Bird Recalls T-Series School Buses for Ignition Interlock Defect

    Micro Bird is recalling 2022-2024 T-Series school buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25034·2024-11-07

    Wolf Dual Fuel ranges with infrared griddles recalled for fire and burn hazards

    Wolf Appliance is recalling about 44,000 Dual Fuel ranges with infrared griddles due to a short-circuit hazard. Liquid spillage can unexpectedly activate the griddle, posing burn and fire risks. No injuries have been reported.

    Product
    Wolf Dual Fuel ranges with infrared griddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25032·2024-11-07

    Guava Roam strollers recalled due to brake failure and fall hazards

    Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.

    Product
    Guava Roam Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V842000·2024-11-07

    Micro Bird Recalls 2023 CT-Series Buses Due to Ignition Interlock Defect

    Micro Bird is recalling 2023 CT-Series buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD CT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25030·2024-11-07

    Dreamgro Lullaby Travel Soothers Recalled Due to Choking Hazard

    Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.

    Product
    Dreamgro Lullaby mermaid travel soothers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25031·2024-11-07

    Kyte Baby Slumber Suits Recalled Due to Flammability Violation, Burn Injury Risk

    Kyte Baby is recalling about 20,500 Slumber Suits sold from November 2022 to March 2024 because they violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. No injuries have been reported.

    Product
    Kyte Baby Slumber Suits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25033·2024-11-07

    Baofali 4-in-1 Microfiber Crib Bumpers Recalled for Suffocation Hazard

    Baofali 4-in-1 Microfiber Crib Safety Bumpers sold on Temu.com violate the federal crib bumper ban and pose a suffocation hazard to infants. About 390 units were sold from June through August 2024.

    Product
    Baofali 4-in-1 Microfiber Crib Safety Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V839000·2024-11-07

    2022-2023 Chevrolet Express and GMC Savana transmission software defect

    GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V843000·2024-11-07

    2024 Hyundai Santa Fe sunshade switch defect increases injury risk

    Hyundai is recalling 34,964 units of the 2024 Santa Fe and Santa Fe Hybrid with faulty switch knobs that may not retract, creating an injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE HYBRID, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V837000·2024-11-06

    PJ TRAILERS LD trailers recalled for incorrectly installed brake axles

    PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.

    Product
    PJ TRAILERS — PJ TRAILERS LD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0089-2025·2024-11-06

    Ginger Chicken Broccoli Salad Kit Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Ginger Chicken Broccoli Salad Kit V due to potential Listeria monocytogenes contamination in the cooked chicken. The product was distributed to 31 states.

    Product
    Item 404790, UPC 13454 38101, Ginger Chicken Broccoli Salad Kit V, 1/6.9625lb. Distributed by Fresh Creative Foods Vista, CA.
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Devices)·Z-0092-2025·2024-11-06

    VasoView HemoPro Vessel Harvesting System Recalled for Silicone Component Detachment

    Maquet Cardiovascular is recalling the VasoView HemoPro Endoscopic Vessel Harvesting System due to silicone detachment from the Harvesting Tool Jaws during use. This FDA Class I recall affects 28,809 units worldwide.

    Product
    VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0088-2025·2024-11-06

    Reser's Caesar Salad Kits Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Caesar Salad Kits due to Listeria monocytogenes contamination in the cooked chicken component. The recall affects 21,098 cases distributed across 31 U.S. states.

    Product
    Item 401311, UPC 13454 35855, Caesar Salad Kit 2/6 lbs. Distributed by Fresh Creative Foods Vista, CA.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-0248-2025·2024-11-06

    Surgical Patties and Strips Recalled for Higher-Than-Expected Endotoxin

    Integra LifeSciences is recalling surgical patties and strips (Model 801449) due to higher-than-expected endotoxin levels in raw materials that may have resulted in out-of-specification finished products.

    Product
    SURG STRP 1/8X6 Model/Catalog Number: 801449. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0270-2025·2024-11-06

    Laryngeal Tube Device Recalled for Unapproved Pediatric Indication

    King Systems Corp. is recalling 21,939 KING LTSD laryngeal tubes nationwide because the device was marketed for pediatric use without proper FDA regulatory clearance. The device was originally approved only for adult use.

    Product
    KING LTSD,SIZE 1,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KLTSD421
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0253-2025·2024-11-06

    Surgical Patties and Strips Recalled for Higher-Than-Expected Endotoxin Levels

    Integra LifeSciences is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw material that may result in out-of-specification finished products. The recall affects 2,056 units distributed worldwide.

    Product
    SURG STRP 1-1/2X6 Model/Catalog Number: 801454. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2025·2024-11-06

    Surgical Patties and Strips Recalled for Out-of-Specification Endotoxin

    Integra LifeSciences is recalling Codman Surgical Patties and Strips (Model 801400) due to higher-than-expected endotoxin levels in raw materials that resulted in out-of-specification finished products.

    Product
    SURG PAT XRAY 1/2X1/2 Model/Catalog Number: 801400. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0247-2025·2024-11-06

    Surgical patties and strips recalled for elevated endotoxin levels

    Integra LifeSciences is recalling surgical patties and strips (Model 801409) used in surgery due to higher-than-expected endotoxin levels detected in raw materials. No illnesses have been reported.

    Product
    SURG PAT XRAY 3X3 Model/Catalog Number: 801409. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0091-2025·2024-11-06

    Asian Style Chicken Stir Fry Kit recalled for Listeria monocytogenes

    Reser's Fine Foods recalled Asian Style Chicken Stir Fry Kits distributed by Fresh Creative Foods due to Listeria monocytogenes contamination in the cooked chicken. 192 cases were distributed across 30 US states.

    Product
    Item 406740, UPC 13454 38316, Asian Style Chicken Stir Fry Kit On Premise With Trays 2/6.5 LB. Distributed by Fresh Creative Foods, Vista, CA.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-0249-2025·2024-11-06

    Surgical patties and strips recalled for endotoxin contamination

    Integra LifeSciences is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw materials. The contamination may have resulted in out-of-specification finished products.

    Product
    SURG STRP 1/4X6 Model/Catalog Number: 801450. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0252-2025·2024-11-06

    Surgical Patties and Strips Recalled for Endotoxin Contamination

    Integra LifeSciences is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw material, which may result in out-of-specification endotoxin in finished products.

    Product
    SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide