The Recall Desk

State

Indiana product recalls

73,598 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,592
Critical
1,908
Severe
2,534
Most recent
2026-10-24

Of the 9,592 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 2,534 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30251–30275 of 83190

  • HighFDA (Devices)·Z-0097-2021·2020-10-21

    Biomet Recalls RingLoc Hip Cups Due to Double Sterilization

    Biomet is recalling 48 RingLoc Bi-Polar Hip System Acetabular Cups because they were gamma sterilized twice, which may compromise functionality and shelf life.

    Product
    (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar Cup, E1 Antioxidant Infused, 28 MM, 41 MM: Item No. 110010458; Lot No. 710930; UDI No. (01) 00880304568747 (17) 230614 (10) 710930 (2) RingLoc Hip system Acetabular Bi-Polar Cup: Acetabular Cup…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0105-2021·2020-10-21

    Cook Inc. Recalls Percutaneous Neonatal Pigtail Nephrostomy Sets

    Cook Inc. is recalling 368 Percutaneous Neonatal Pigtail Nephrostomy Sets because the indwell time is decreasing from 4 months to 4 weeks.

    Product
    Percutaneous Neonatal Pigtail Nephrostomy Set, Reference Part Number 080106, Order Number G14508. The set contains a 22 gage, 5 cm Chiba Needle; an 18 gage, 5 cm trocar needle; an .038-inch (.97 mm) diameter, 30 cm PTFE-coated stainless steel; a 5, 6, and 7 French, 10 cm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0107-2021·2020-10-21

    Ezycare Disposable Face Masks Recalled for Mislabeling as Non-Medical

    FDA is recalling Ezycare disposable face masks because they were labeled as non-medical but distributed to customers expecting medical use.

    Product
    Ezycare Face Mask, Disposable Non Medical Face Masks - Product Usage: marketed under face mask umbrella EUA as source control.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0093-2021·2020-10-21

    Biomet Shoulder Prosthesis Baseplate Packaging Error Recall

    Biomet is recalling 3 units of Comprehensive Reverse Shoulder Glenosphere Mini Baseplates due to packaging errors where components may be missing or duplicated.

    Product
    Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis item: 010000589 - Product Usage: intended to serve as the foundation for the reverse shoulder prosthesis head (glenosphere).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0106-2021·2020-10-21

    Cook Inc. Recalls Pediatric Nephrostomy Stent Sets Due to Labeling Update

    Cook Inc. is recalling 380 Pediatric Nephrostomy Stent Sets because the indwell time is decreasing from 4 months to 4 weeks. The Instructions for Use are being updated to reflect this change.

    Product
    Pediatric Nephrostomy Stent Set, Reference Part Numbers 080208-S6 and 080208-S7, Order Numbers G15034 and G15035. The set contains a radiopaque pigtail catheter and stent, retention disc with pull tie, and a 10 French, 30 cm polyvinylchloride connecting tube with one-way…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0104-2021·2020-10-21

    Roche Recalls Albumin Gen.2 Reagents Due to Cross-Contamination

    Roche Diagnostics is recalling Albumin Gen.2 reagents due to cross-contamination causing low quality recovery and invalid calibrations.

    Product
    Albumin Gen.2, Catalog 05166861190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0103-2021·2020-10-21

    Roche Recalls Tina-quant Complement C4 Reagents Due to Quality Issues

    Roche Diagnostics is recalling 180 units of Tina-quant Complement C4 reagents due to cross-contamination causing invalid calibrations.

    Product
    Tina-quant Complement C4 ver.2, Catalog 05991994190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V646000·2020-10-19

    Mitsubishi Fuso Trucks Recalled for Loose Exhaust Studs and Fire Risk

    Mitsubishi Fuso is recalling 2019-2021 FEC7T, FEC9T, and FECZT trucks because loose exhaust studs may allow hot gases to leak, increasing fire risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T, FEC9T, FECZT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V645000·2020-10-19

    Mitsubishi Fuso Trucks Recalled for Brake Booster Vacuum Pump Defect

    Mitsubishi Fuso is recalling 2019-2021 FEC7T, FEC9T, and FECZT trucks because heat from the exhaust manifold may crack the brake booster vacuum pump diaphragm, potentially disabling power brake assist.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T, FEC9T, FECZT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V644000·2020-10-19

    Audi Recalls One 2020 Q3 for Driver's Seat Frame Bolt Defect

    Audi is recalling one 2020 Q3 because the driver's seat frame may be incorrectly bolted to the seat rail, increasing injury risk in a crash.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E079000·2020-10-17

    Fuel Delivery Module Recall Due to Potential Stalling Risk

    Continental Automotive Systems is recalling Vitesco NG2 Fuel Delivery Modules where a plastic burr may block the mixing tube, causing insufficient fuel supply and vehicle stalling.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E078000·2020-10-16

    Weldon V-Mux Vista IV LCD Displays Recalled for Electrical Lockup

    Akron Brass is recalling Weldon V-Mux Vista IV LCD displays used in emergency vehicles because they may lock up due to voltage spikes, potentially delaying emergency efforts.

    Product
    ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V639000·2020-10-15

    GM Recalls 2020 SUVs for Fuel Pump Defect Causing Engine Stalls

    General Motors is recalling 2,781 2020 Buick, Cadillac, Chevrolet, and GMC SUVs because a fuel pump defect may cause the engine to stall without warning.

    Product
    CADILLAC — CADILLAC, BUICK, CHEVROLET XT5, XT6, ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V582000·2020-10-15

    Prime-Time Recalls 2014-2019 Ram ProMaster Paratransit Vehicles

    Prime-Time Specialty Vehicles is recalling 2014-2019 Ram ProMaster Paratransit vehicles because the transmission shifter cable may disconnect, causing unintended movement.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V638000·2020-10-15

    GM Recalls 2014-2016 Chevrolet SS and Caprice PPV for Seat Belt Defect

    General Motors is recalling 1,788 vehicles because a previous repair may have been improper, causing the driver's seat belt tensioner cable to fatigue and separate.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS, CAPRICE POLICE PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21702·2020-10-15

    Peloton Recalls PR70P Bike Pedals Due to Laceration Hazard

    Peloton is recalling PR70P clip-in pedals fitted on bikes sold between July 2013 and May 2016 because they can break unexpectedly, causing laceration injuries.

    Product
    PR70P Clip-In Pedals fitted on Peloton bikes (sold between July 2013 and May 2016)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V637000·2020-10-15

    Genie Recalls 2020 TZ-34 and TZ-50 Trailer-Mounted Boom Lifts

    Genie is recalling 2020 TZ-34 and TZ-50 trailer-mounted boom lifts because under-tightened bolts may affect stability and increase injury risk.

    Product
    GENIE — GENIE TZ-50, TZ-34
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21703·2020-10-15

    Homerygardens Extension Cord Splitters Recalled for Fire Hazard

    Sales BSD is recalling Homerygardens extension cord splitters because the wire size cannot handle the appropriate amp load, posing a fire hazard.

    Product
    Homerygardens™ 4-Outlet, 6-Foot Long Indoor and Outdoor Extension Cord Splitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide