The Recall Desk

State

Indiana product recalls

73,376 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,587
Critical
1,913
Severe
2,528
Most recent
2026-09-30

Of the 9,587 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,528 (26%) are Severe.

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20601–20625 of 82963

  • ModerateFDA (Devices)·Z-1807-2022·2022-10-05

    Wound Dressing Units Recalled Due to Storage Temperature Excursions

    KerraCel Ag wound dressing units distributed between June and September 2021 are being recalled due to facility temperature excursions that may have affected product effectiveness. The FDA states no adverse health consequences are likely.

    Product
    3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1806-2022·2022-10-05

    McKesson Wound Dressing Products Recalled for Temperature Exposure

    McKesson wound dressing products distributed nationwide are being recalled due to exposure to elevated temperatures during storage that may have reduced their effectiveness. No adverse health consequences have been reported.

    Product
    a. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WOUND GELLING FIBERHIGH-ABSRB 4"X4 3/4" (10/BX) Catalog #87400. b. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WND GELLING FIBER HIABSRB AG 4X4.75 (10/BX 10BX/CS Catalog #177400. c. ADVANCED MEDICAL SOLUTIONS McKesson…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1851-2022·2022-10-05

    Leica Surgical Microscopes: Photodiode Defect Causes Inaccurate Illumination

    Leica Microsystems is recalling 32 surgical operating microscopes due to a photodiode component defect that produces inaccurate illumination adjustment when BrightCare Plus with Luxmeter is used.

    Product
    Leica Surgical Operating Microscopes, PROvido Part Numbers: a. 10448976, b. 10448950
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1802-2022·2022-10-05

    Medical Monofilament Testing Devices Recalled for Temperature Excursion

    Mckesson Medical-Surgical is recalling monofilament sensory testing devices (13 units) due to temperature excursions during June-August 2021. Heat exposure may have compromised device effectiveness.

    Product
    Medical Monofilament Manufacturing MONOFILIMENT TEST, SENSORY F/FOOT 10GM (40/PK) Model Number: AM140
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1798-2022·2022-10-05

    AquaGuard Wound Dressing Recall Due to Facility Temperature Excursions

    TIDI Products AquaGuard wound dressings received June–September 2021 were exposed to elevated storage temperatures that may have impacted product effectiveness. The FDA states adverse health consequences are unlikely.

    Product
    a. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR 7X7 (5/PK) 9CENCO Catalog #68751510104. b. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR BARR 10X12 (5/BX) Catalog #68751510105
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1796-2022·2022-10-05

    Mckesson DermaCol Collagen Dressings Recalled for Storage Temperature Excursion

    Mckesson recalls DermaCol collagen dressings exposed to temperature excursions during storage (June-August 2021). FDA stated adverse health consequences are unlikely.

    Product
    a. DERMARITE INDUSTRIES DermaCol Collagen Dressing DermaCol Without Border Collagen / Sodium Alginate / Carboxyl Methylcellulose (CMC) / Ethylenediamine-tetraacetic Acid (EDTA) 4 X 4 Inch 10 Count Model Number: 00303E. b. DERMARITE INDUSTRIES DermaCol Ag Silver Collagen…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V738000·2022-10-04

    Contract Manufacturer Recalls 2023 Trailers With Incorrect Axle Size

    Contract Manufacturer is recalling 2023 trailers because an incorrect axle size may have been installed, posing a crash risk if the axle breaks.

    Product
    CONTRACT MANUFACTURER — CONTRACT MANUFACTURER EQ14-17+3, TH10-20BK4CR, EQ16-17+3, TU10-20BK4CR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V736000·2022-10-04

    Blue Bird Recalls 2013-2021 Vision School Buses for Fuel Leak Risk

    Blue Bird is recalling 2013-2021 Vision school buses with Ford 6.8L LPG engines because a damaged fuel line may leak, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V737000·2022-10-04

    2022-2023 Coachmen Recreational Vehicles Recall: Unintended Awning Movement

    Forest River is recalling certain 2022-2023 Coachmen recreational vehicles with a software issue that may cause the awning to unintentionally extend or retract while parked, increasing injury risk. Owners should contact dealers for a free ECM software update.

    Product
    COACHMEN — COACHMEN GALLERIA, NOVA, BEYOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V735000·2022-10-03

    East Texas Recalls 2021 Tank Trailers Due to Axle Weld Defect

    East Texas Trailer is recalling 2021 Tank trailers because a defective axle weld may crack or separate, increasing crash risk.

    Product
    EAST TEXAS — EAST TEXAS TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E085000·2022-09-30

    Meritor Recalls Front Non-Drive Steer Axles Due to Tie Rod Clamp Cracking

    Meritor is recalling certain Front Non-Drive Steer Axles because improperly heat-treated tie rod clamps may crack and separate, potentially causing a sudden loss of steering.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V734000·2022-09-30

    Great Dane Recalls 2023 Trailers Due to Brake Pad Retaining Clip Issue

    Great Dane is recalling 2023 Champion and Everest trailers because a loose brake pad retaining clip may reduce braking performance or cause a flat tire.

    Product
    GREAT DANE — GREAT DANE EVEREST, CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V751000·2022-09-30

    Braun Ambulances Recall 2018-2022 Models Due to Rear Door Bolt Issue

    Braun Ambulances is recalling 2018-2022 models because rear door striker bolts may dislodge, potentially causing the door to open during a crash.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES SUPER CHIEF, EXPRESS PLUS, LIBERTY, TLC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V732000·2022-09-30

    Mercedes-Benz Recalls GLS Models Due to Third-Row Seatback Lock Failure

    Mercedes-Benz is recalling specific GLS models because third-row seatback locks may fail in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 580 4MATIC, GLS 450 4MATIC, AMG GLS63, GLS580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V728000·2022-09-30

    Crossroads and Dutchmen Trailers Recalled for Loose Axle U-Bolts

    Keystone RV is recalling 2021-2022 Crossroads Redwood, Dutchmen Voltage, and Yukon trailers for improperly tightened axle U-bolts that may cause loss of vehicle control and crash risk.

    Product
    CROSSROADS — CROSSROADS, DUTCHMEN REDWOOD, VOLTAGE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V729000·2022-09-30

    2021-2022 Forest River Travel Trailers: Fresh Water Tank Dislodgement

    Forest River is recalling 2021-2022 Ozark, Wildwood, and Salem travel trailers because the fresh water tank may dislodge when full or overfilled, creating a road hazard and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM, OZARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V731000·2022-09-30

    Ford F-53 Rear Stabilizer Brackets May Separate from Vehicle

    Ford is recalling 2020-2021 F-53 recreational vehicles because rear stabilizer bar attachment brackets may break and separate, creating a road hazard and increasing crash risk. Dealers will inspect and replace the brackets free of charge.

    Product
    FORD — FORD F53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V730000·2022-09-30

    2022 Ford Maverick brake lights may illuminate unintended due to ABS defect

    Ford is recalling 2022 Maverick vehicles with an ABS module defect that may cause brake lights to illuminate without driver input. This could confuse other drivers and increase crash risk.

    Product
    FORD — FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V733000·2022-09-30

    2020 Mercedes-Benz CLS450 improperly secured battery defect recall

    Mercedes-Benz is recalling 2019-2022 CLS450 and related models. The 12V battery in the trunk may not be properly secured, which could cause electrical failure and disable safety features like the emergency call system, hazard lights, and automatic door locks in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, AMG E53, AMG CLS53, CLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22235·2022-09-29

    Custom Elevator Residential Elevators Recalled for Child Entrapment Hazard

    Custom Elevator is recalling residential elevators due to a hazardous gap between the exterior landing door and interior car door that can trap young children. One child died from entrapment in July 2021.

    Product
    Residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22234·2022-09-29

    Cambridge Elevating Residential Elevators Recalled for Child Entrapment Hazard

    Cambridge Elevating residential elevators may have a hazardous gap between exterior and interior doors that can trap young children, posing a risk of serious injury or death when the elevator moves. About 1,700 units sold nationwide from 1991 through August 2022 are affected.

    Product
    Residential elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22E083000·2022-09-29

    Chrysler Recalls Mopar Headlamp Assemblies for Dim Amber Reflectors

    Chrysler is recalling specific Mopar headlamp assemblies because the amber side reflex reflector may not reflect brightly enough, potentially reducing vehicle visibility.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V727000·2022-09-29

    2022 Lucid Air: Tow Eye Bracket Detachment Risk During Towing

    Lucid is recalling certain 2022 Air vehicles where the front tow eye bracket may be inadequately attached to the subframe and can detach during towing. This could separate the vehicle from the tow truck, increasing crash risk.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide