The Recall Desk

State

Indiana product recalls

73,741 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,596
Critical
1,908
Severe
2,534
Most recent
2026-10-28

Of the 9,596 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 9,596 recalls whose distribution notice names Indiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38326–38350 of 83337

  • HighFDA (Food)·F-1231-2019·2019-04-10

    Fungi Perfecti Recalls Host Defense Blood Sugar Supplement for Undeclared Wheat

    Fungi Perfecti LLC is recalling Host Defense MycoBotanicals Blood Sugar dietary supplements because they contain undeclared wheat. The recall affects 11,042 bottles distributed in the US, Canada, and Norway.

    Product
    Host Defense MycoBotanicals Blood Sugar, dietary supplement, 500mg capsules, 60 ct per bottle, serving size 2 capsules per day. UPC: 6 33422 70474 6 (distributed in US) UPC: 8 22078 71303 9 (distributed in Canada) The product is labeled in parts: "***HOST DEFENSE MYCO…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1077-2019·2019-04-10

    Morphine Sulfate API Recalled for Microbial Contamination Out of Specification

    Johnson Matthey Inc. is recalling Morphine Sulfate USP Milled API due to bioburden out of specification results.

    Product
    Morphine Sulfate USP Milled, Active Pharmaceutical Ingredient, Rx only, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2019·2019-04-10

    Beckman Coulter UniCel DxI 600 and 800 Systems Recalled for Software Error

    Beckman Coulter is recalling UniCel DxI 600 and 800 systems due to a software scheduling error that can cause incorrect immunoassay results.

    Product
    The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog Numbers: A30260, A71460, A71461, A92060. Unicel DxI 800 Catalog Numbers: 973100, A71456, A71457, A84545, A25288, A25285.
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Drugs)·D-1078-2019·2019-04-10

    KRS Global Biotechnology Recalls Repinephrine IV Bags Due to Labeling Error

    KRS Global Biotechnology is recalling 190 bags of Repinephrine 16 mg IV solution due to a label mix-up. The product was distributed nationwide.

    Product
    NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF), 16 mg / 250 mL, 250 mL IV bag, Rx only, KRS Global Biotechnology: 791 Park of Commerce Blvd., Boca Raton, FL 33487. NDC 3321678343
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1075-2019·2019-04-10

    Abbott ARCHITECT Creatine Kinase IVD Recalled for Stability Issues

    Abbott Laboratories is recalling specific lots of ARCHITECT Creatine Kinase IVD kits due to a stability issue that may cause error codes or out-of-range quality control results.

    Product
    Abbott ARCHITECT Creatine Kinase, IVD, REF 7D63-21.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1074-2019·2019-04-10

    Jubilant Cadista Recalls Pantoprazole Sodium Tablets Due to Discoloration

    Jubilant Cadista Pharmaceuticals is recalling 12,960 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on the tablet edges.

    Product
    Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx Only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801; NDC 59746-284-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1072-2019·2019-04-10

    Pfizer Recalls Clindamycin Injection Vials Due to Impurity Failures

    Pfizer is recalling specific lots of Clindamycin Injection due to high out-of-specification impurity results at the 24-month time point.

    Product
    Clindamycin Injection, USP, 900 mg/6 mL (150 mg/mL), 6 mL vial, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA. NDC 47781-621-94
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1069-2019·2019-04-10

    Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures

    Pfizer is recalling specific lots of Cleocin Phosphate injection because high levels of impurities were found at the 24-month time point.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1071-2019·2019-04-10

    Pfizer Recalls Clindamycin Injection Due to Impurity Specification Failures

    Pfizer is recalling specific lots of Clindamycin Injection because high out-of-specification impurities were found at the 24-month time point.

    Product
    Clindamycin Injection, USP, 600 mg/ 4 mL (150 mg/mL), 4 mL vials, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC 47781-620-94
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1070-2019·2019-04-10

    Pfizer Recalls Clindamycin Injection Vials Due to Impurity Failures

    Pfizer is recalling specific lots of Clindamycin Injection because high levels of impurities were found at the 24-month time point.

    Product
    Clindamycin Injection, USP, 300 mg/ 2 mL (150 mg/mL), 2 mL vials, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA.,NDC 47781-619-94
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1079-2019·2019-04-10

    KRS Global Biotechnology Recalls NORepinephrine IV Bags Due to Labeling Error

    KRS Global Biotechnology is recalling 433 bags of NORepinephrine 4 mg in 5% Dextrose due to a label mix-up. The product was distributed nationwide.

    Product
    NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF), 4 mg / 250 mL, 250 mL IV bag, Rx only, KRS Global Biotechnology: 791 Park of Commerce Blvd., Boca Raton, FL 33487. NDC 3321674481
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1076-2019·2019-04-10

    Abbott ARCHITECT Creatine Kinase IVD Recalled for Stability Issues

    Abbott Laboratories is recalling 30 kits of ARCHITECT Creatine Kinase IVD due to a stability issue that may cause error codes or out-of-range quality control results.

    Product
    Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1074-2019·2019-04-10

    Abbott Recalls CELL-DYN Emerald Analyzers Due to Quality Control Errors

    Abbott Laboratories is recalling 6,353 CELL-DYN Emerald analyzers worldwide because they may generate incorrect low quality control results for red blood cells and platelets.

    Product
    CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro diagnostic use in the clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1068-2019·2019-04-10

    Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures

    Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurity levels were detected at the 24-month time point.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1088-2019·2019-04-10

    Beaver Visitec Recalls Micro Knife 5.0mm Due to Misprinted Expiration Date

    Beaver Visitec is recalling 97 boxes of Micro Knife 5.0mm 30° instruments because the expiration date was misprinted as the lot number.

    Product
    Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1067-2019·2019-04-10

    Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures

    Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurities were detected at the 24-month time point.

    Product
    CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V283000·2019-04-09

    Proterra Recalls 2015-2018 Catalyst Buses Due to Brake Fire Risk

    Proterra is recalling 2015-2018 Catalyst 40 buses because a clogged tow fitting cap can cause rear brakes to overheat and catch fire.

    Product
    PROTERRA — PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V282000·2019-04-09

    Peterbilt 520 Recall: Undersized Wires May Cause Engine Shutdown

    PACCAR is recalling 2017-2020 Peterbilt 520 trucks because undersized wires may overheat and melt, potentially causing an unexpected engine shutdown and increasing crash risk.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V281000·2019-04-09

    Horton Ambulances Recalled for Reversed Backup Camera Image

    Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    HORTON — HORTON TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V284000·2019-04-09

    Daimler Recalls 2019 Sprinter Vans for Headlight Sensor Calibration Issues

    Daimler Vans USA is recalling 2019 Freightliner and Mercedes-Benz Sprinter vans because the headlamp range adjustment sensor may not be calibrated, potentially affecting driver visibility.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V276000·2019-04-09

    AEV TraumaHawk Ambulances Recalled for Reversed Backup Camera Image

    Halcore Group is recalling 2016-2019 AEV TraumaHawk ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V280000·2019-04-09

    Pierce Frontline Vehicles Recalled for Brake Light Wiring Defect

    Pierce is recalling 2018-2019 Frontline C-35X, C-25, C-45X-3, and Encore Rescue vehicles because brake lights may illuminate without the pedal being pressed.

    Product
    FRONTLINE — FRONTLINE C-25, C-35X, ENCORE RESCUE, C-45X-3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19102·2019-04-09

    Marpac Recalls GO Travel Sleep Sound Machines Due to Burn Hazard

    Marpac is recalling GO travel sleep sound machines because the internal battery can leak and cause an electrical short, posing a burn hazard.

    Product
    GO travel sleep sound machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V279000·2019-04-08

    Load Trail Recalls 2018-2019 Dump Trailers Due to Bolt Failure Risk

    Load Trail is recalling 2018-2019 dump trailers because bolts on the hydraulic cylinder can break under heavy loads, causing the dump box to lower rapidly.

    Product
    LOAD TRAIL — LOAD TRAIL TANDEM AXLE DUMP, TRIPLE AXLE DUMP
    Category
    Vehicle
    Distribution
    Distributed nationwide