The Recall Desk

State

Indiana product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39326–39350 of 83404

  • SevereFDA (Devices)·Z-0855-2019·2019-02-27

    Philips PageWriter TC30 ECG Devices Recalled for Overheating and Ignition Risk

    Philips is recalling PageWriter TC30 ECG devices because end-of-life batteries may overheat, melt the case, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30, Product 860306, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0504-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA labs found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP, 100 mg/12.5 mg, a) 90-count bottle (NDC: 13668-117-90), b) 1000-count bottle (NDC: 13668-117-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0505-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP 50 mg/12.5 mg, a) 90-count bottle (NDC: 13668-116-90), b) 1000-count bottle (NDC: 13668-116-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0858-2019·2019-02-27

    Philips PageWriter TC Cardiograph Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC70 w/o trolley Government Bundle, Product 860353, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0502-2019·2019-02-27

    Torrent Pharma Recalls Losartan Potassium Tablets Due to NDEA Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count bottle (NDC: 13668-409-30), b) 90-count bottle (NDC: 13668-409-90), c) 1000-count bottle (NDC: 13668-409-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0509-2019·2019-02-27

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to CGMP Deviations

    ICU Medical Inc. is voluntarily recalling 475,320 bags of 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0853-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19074·2019-02-27

    Harbor Freight Recalls Greenwood Propane Torches Due to Burn Hazard

    Harbor Freight Tools is recalling Greenwood propane torches because the trigger can fail to disengage, posing a burn hazard. One burn injury has been reported.

    Product
    Greenwood propane torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0942-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Due to Salmonella Risk

    Ardent Mills is voluntarily recalling specific lots of Members Mark Self-Rising Flour because they may be contaminated with Salmonella.

    Product
    MEMBERS MARK SELF RISE FLR 25LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V137000·2019-02-27

    Freightliner Recalls 2020 Cascadia Trucks for Incorrect Gear Display

    Daimler Trucks is recalling 2020 Freightliner Cascadia trucks because the instrument cluster may incorrectly display 'Neutral' when the truck is in gear, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E017000·2019-02-27

    Specialty Manufacturing Recalls Transpec T287X Series Glass Roof Hatches

    Specialty Manufacturing is recalling Transpec T287X Series glass roof hatches because temperature and vibration stresses may cause the tempered glass to shatter, posing an injury risk to passengers.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0939-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Lots for Potential Salmonella Contamination

    Ardent Mills is voluntarily recalling specific lots of self-rising flour due to potential Salmonella contamination. The affected products were distributed nationwide.

    Product
    ARDENT H&R SR FLR, 25LB, 50 LB, and 25LB (PC)-309951, packaged in paper bags, Store at Ambient Temperature
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0849-2019·2019-02-27

    Baxter AMIA Automated Peritoneal Dialysis System Software Recall

    Baxter is recalling 7,688 AMIA Automated Peritoneal Dialysis Systems due to a software defect that may cause shortened dwell times during therapy.

    Product
    AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution exchanges in the treatment of adult renal failure patients undergoing Peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0941-2019·2019-02-27

    Ardent Mills Recalls Self-Rising Flour Due to Salmonella Risk

    Ardent Mills is voluntarily recalling certain lots of Westcreek Self-Rising Flour because they may be contaminated with Salmonella.

    Product
    WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0507-2019·2019-02-27

    Dr. Reddy's Recalls Divalproex Sodium Tablets for Dissolution Failure

    Dr. Reddy's is recalling 10,656 bottles of Divalproex Sodium Extended-release Tablets because they failed to meet dissolution specifications.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V133000·2019-02-27

    Triumph Recalls Motorcycles Due to Clutch Cable Wiring Damage Risk

    Triumph is recalling specific 2016-2019 motorcycles because the clutch cable may damage wiring, potentially causing electrical failures or engine stalling.

    Product
    TRIUMPH — TRIUMPH SCRAMBLER, STREET TWIN, BONNEVILLE T120 BLACK, STREET CUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V134000·2019-02-27

    Lexus Recalls 2018 LS Models for Run-Flat Tire Defect

    Toyota is recalling 2018 Lexus LS vehicles because run-flat tires may have cracked reinforcement layers, potentially causing tread separation and affecting vehicle stability.

    Product
    LEXUS — LEXUS LS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V140000·2019-02-27

    Midway Recalls One 2016 Freightliner Sprinter 3500 Wheelchair Lift Vehicle

    Midway Specialty Vehicles is recalling one 2016 Freightliner Sprinter 3500 because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2019·2019-02-27

    Ortho-Clinical Diagnostics Recalls VITROS VALP Reagent Packs Due to Negative Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products VALP Reagent Packs because they may produce negative bias results when measuring valproic acid.

    Product
    VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 6801710 INTENDED USE: For in vitro diagnostic use only. VITROS Chemistry Products VALP Reagent is used on the VITROS 5,1 FS Chemistry System, the VITROS 4600 Chemistry System and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2019·2019-02-27

    Boston Scientific Recalls Mislabelled Stingray Guidewires for Coronary Procedures

    Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.

    Product
    Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0513-2019·2019-02-27

    Lupin Recalls Lovastatin Tablets Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Lovastatin 40 mg tablets because the drug substance used was out of specification for impurity results.

    Product
    LOVASTATIN — LOVASTATIN (LOVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide