The Recall Desk

State

Indiana product recalls

73,817 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,598
Critical
1,908
Severe
2,536
Most recent
2026-11-04

Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45526–45550 of 83415

  • ModerateFDA (Devices)·Z-0188-2018·2017-12-06

    Medtronic Recalls Everflex Self-Expanding Peripheral Stents Due to Labeling Error

    Medtronic is recalling 21 units of Everflex Self-Expanding Peripheral Stents because the stent length on the label may not match the actual stent length.

    Product
    Everflex Self-Expanding Peripheral Stent with Entrust Delivery System Intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 140 mm in length in the native Superficial Femoral Artery (SFA) and/or proximal popliteal arteries…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·18047·2017-12-05

    Netgear Recalls Outdoor Camera Power Adapters Due to Fire Hazard

    Netgear is recalling VMA4700 power adapters for Arlo outdoor cameras because water leakage can cause short circuits, melting, and fire.

    Product
    Power adapters for outdoor Arlo cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18053·2017-12-05

    Metabo Recalls Rat Tail Angle Grinders Due to Laceration Hazard

    Metabo is recalling specific rat tail angle grinders because the on-off switch can lock in the on position, posing a laceration hazard.

    Product
    Rat tail angle grinders with brake
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V776000·2017-12-04

    Burch Recalls 1984 Evans Cargo Tank Trailers Due to Brake Caliper Bolts

    Burch Tank and Truck is recalling 1984 Evans Cargo Tank trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.

    Product
    EVANS — EVANS CARGO TANK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V778000·2017-12-04

    Triple E RV Recalls 2016-2018 Wonder Motorhomes for Seat Bolt Issue

    Triple E RV is recalling 2016-2018 Wonder motorhomes because improperly tightened passenger seat bolts may fail in a crash, increasing injury risk.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V777000·2017-12-04

    Temsa Recalls 2017-2018 Buses Due to Fire Suppression Chemical Contamination

    Temsa is recalling 2017-2018 TS30, TS35E, and TS45 buses because the fire suppression system may contain contaminated dry chemical, which could discharge improperly and increase injury risk.

    Product
    TEMSA — TEMSA TS45, TS30, TS35E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V775000·2017-12-01

    Ford Recalls 2018 Expedition Vehicles for Seat Back Bolt Defect

    Ford is recalling 2018 Expedition vehicles because second-row outboard seats may have improperly installed bolts or excessive forward adjustment, increasing injury risk in a crash.

    Product
    FORD — FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V772000·2017-12-01

    MV Agusta Recalls 2017 Brutale 800 Dragster RR for Rear Wheel Spokes

    MV Agusta is recalling 45 2017 Brutale 800 Dragster RR motorcycles because rear wheel spokes may loosen, potentially affecting handling and increasing crash risk.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18051·2017-12-01

    Camso Recalls Dirt to Snow Bike Conversion Kits Due to Crash Hazards

    Camso is recalling DTS 129 conversion kits because a brake pin can loosen, posing a crash or impact hazard. No injuries have been reported.

    Product
    Camso dirt to snow bike conversion kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V773000·2017-12-01

    Kia Recalls 2012-2014 Forte Models Due to Brake Pedal Stopper Pad Defect

    Kia is recalling 2012-2014 Forte and Forte Koup vehicles because a deteriorating brake pedal stopper pad may keep brake lights on or allow shifting without pressing the brake pedal.

    Product
    KIA — KIA FORTE KOUP, FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V769000·2017-11-30

    Hyundai Recalls 2013-2014 Elantra for Brake Pedal Stopper Pad Defect

    Hyundai is recalling 2013-2014 Elantra vehicles because a deteriorating brake pedal stopper pad can cause brake lights to stay on and allow shifting out of park without pressing the brake pedal.

    Product
    HYUNDAI — HYUNDAI ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18049·2017-11-30

    Synodrin Pain Relieving Cream Recalled for Non-Child-Resistant Packaging

    Natural Solutions for Life is recalling Synodrin Pain Relieving Cream because the jar caps are not child-resistant, posing a poisoning risk to young children.

    Product
    Maximum Strength Synodrin Pain Relieving Cream with Lidocaine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18050·2017-11-30

    Flos Recalls Pendant Light Fixtures Due to Impact Injury Hazard

    Flos Inc. is recalling specific Romeo Moon and Romeo Louis II pendant light fixtures because the internal glass diffuser can detach and fall, posing an impact injury hazard.

    Product
    Pendant light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0141-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Trays Due to Design Incompatibility

    Exactech is recalling 537 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 4F/4T, Beta, Ref 208-04-44, Sterile, RX. .
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0167-2018·2017-11-29

    Zimmer Biomet ROSA Brain 3.0.0 Software Recall for Communication Errors

    Zimmer Biomet is recalling 18 units of ROSA Brain 3.0.0 software due to communication errors between software components and the controller.

    Product
    ROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0140-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility

    Exactech is recalling 547 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 4F/4T, Alpha, Ref 208-04-43, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0132-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Trays Due to Design Incompatibility

    Exactech is recalling 665 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 1F/1T & 2F/1T, Beta, Ref 208-04-22, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0135-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility

    Exactech, Inc. is recalling 733 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 3F/2T, Alpha, Ref 208-04-31, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0137-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility

    Exactech is recalling 720 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 3F/3T, Beta, Ref 208-04-34, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0143-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility

    Exactech is recalling 333 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 5F/4T, Beta, Ref 208-04-52, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states