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.

46226–46250 of 83415

  • ModerateFDA (Devices)·Z-3121-2017·2017-09-20

    Leica Biosystems Recalls Glypican-3 Antibody Due to Temperature Deviation

    Leica Biosystems Richmond Inc. is recalling three units of Glypican-3 (1G12 Mab) antibody because a delay in transit may have caused the product to be stored outside of defined temperature requirements.

    Product
    Cell Marque, Glypican-3 (1G12 Mab), 7 mL, REF PA0800, IVD, The antibody is intended for in vitro diagnostic (IVD) use. Glypican-3 (1G12) Mouse Monoclonal Primary Antibody is intended for laboratory use in the detection of the Glypican-3 protein in formalin-fixed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3115-2017·2017-09-20

    Implant Direct Sybron Recalls Guided Surgery Handle Kits Due to Dimensional Defect

    Implant Direct Sybron is recalling 84 Guided Surgery Handle Kits because the 2.3mm drill guide inserts have a smaller inside diameter than specifications require.

    Product
    Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows clinicians to drill through a surgical guide to create an osteotomy for implant placement with the precision and accuracy as designed with treatment planning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3118-2017·2017-09-20

    Beckman Coulter Recalls Sekisui Acetaminophen Reagent Due to Carryover

    Beckman Coulter is recalling 320 units of Sekisui Acetaminophen reagent because carryover from ACTH reagent may cause falsely elevated Lipase results on the AU 680 analyzer.

    Product
    Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K , Ref. 506-30. The firm names on the label are Sekisui Diagnostics (UK) Limited, United Kingdom, and Sekisui Diagnostics P.E.I. Inc., Canada. Used in laboratory testing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3131-2017·2017-09-20

    Mako Surgical Recalls Robotic Arm Interactive Orthopedic System Software

    Mako Surgical Corporation is recalling the Total Hip Application software for the RIO system due to a display error that may hide essential constants.

    Product
    Total Hip Application (THA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is intended to assist the surgeon in providing software define spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3126-2017·2017-09-20

    Leica Biosystems Recalls SOX-10 Antibody Due to Temperature Excursion

    Leica Biosystems Richmond Inc. is recalling 37 units of SOX-10 (Polyclonal) antibody because a delay in transit may have caused the product to be stored outside of defined temperature requirements.

    Product
    Cell Marque, SOX-10 (Polyclonal), 7 mL, REF PA0813, IVD, This antibody is intended for in vitro diagnostic (IVD) use. SOX-10 Rabbit Polyclonal Primary Antibody is intended for laboratory use in the detection of the SOX-10 protein in formalin-fixed, paraffin-embedded tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3124-2017·2017-09-20

    Leica Biosystems Recalls Napsin A Antibody Due to Temperature Excursion

    Leica Biosystems Richmond Inc. is recalling 33 units of Napsin A (MRQ-60 Mab.) antibody because a delay in transit may have caused the product to be stored outside of defined temperature requirements.

    Product
    Cell Marque, Napsin A (MRQ-60 Mab.), 7 mL, REF PA0805, IVD, The antibody is intended for in vitro diagnostic (IVD) use. Napsin A (MRQ-60) Mouse Monoclonal Primary Antibody is intended for laboratory use in the detection of the Napsin A protein in formalin-fixed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3122-2017·2017-09-20

    Leica Biosystems Recalls MiTF Antibody Due to Temperature Deviation

    Leica Biosystems Richmond Inc. is recalling 10 units of Microphthalmia Transcription Factor (MiTF) antibody because a transit delay caused the product to be stored outside required temperature ranges.

    Product
    Cell Marque, Microphthalmia Transcription Factor (MiTF) (C5/D5 Mab.), 7 mL, REF PA0803, IVD, The antibody is intended for in vitro diagnostic (IVD) use. The Microphthalmia Transcription Factor (MiTF) (C5/D5) antibody is intended for qualified laboratories to qualitatively…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3119-2017·2017-09-20

    bioMerieux Recalls eMAG System Due to Manufacturing Anomalies

    bioMerieux, Inc. is recalling 15 eMAG System units in the US and 11 countries due to anomalies identified during manufacturing controls.

    Product
    eMAG System, Ref 418591 It is an In Vitro Diagnostic Medical device intended for the automated isolation (purification and concentration) of total nucleic acids (RNA/DNA) from biological specimens, with liquid and homogeneous properties (as part of their natural…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1134-2017·2017-09-20

    Ascend Amlodipine Besylate Tablets Recalled for Foreign Tablet Presence

    Ascend Laboratories is recalling 10 mg Amlodipine Besylate tablets because 2.5 mg tablets were found mixed in the bottles.

    Product
    AMLODIPINE BESYLATE — AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3125-2017·2017-09-20

    Leica Biosystems Recalls PAX8 Antibody Due to Temperature Deviation

    Leica Biosystems Richmond Inc. is recalling five units of PAX8 antibody because a transit delay may have caused the product to be stored outside required temperature limits.

    Product
    Cell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in vitro diagnostic (IVD) use. PAX-8 (MRQ-50) Mouse Monoclonal Primary Antibody is intended for laboratory use in the detection of the PAX-8 protein in formalin-fixed, paraffin-embedded tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1138-2017·2017-09-20

    Medline Recalls Mislabelled Vitamin A&D Ointment Packets

    Medline Industries is recalling Vitamin A&D Ointment packets that are incorrectly labeled as petroleum jelly. The outer boxes are correctly labeled.

    Product
    Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant, NET Wt. 0.18 OZ (5g), Manufactured for Medline Industries, Inc., Northfield, IL 60093 USA. NDC: 53329-090-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3129-2017·2017-09-20

    Fujifilm Endoscope Corrective Action Following FDA Inspection

    Fujifilm Medical Systems U.S.A., Inc. is conducting a corrective action for specific endoscope models following an FDA inspection.

    Product
    Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3123-2017·2017-09-20

    Leica Biosystems Recalls MSH6 Antibody Due to Temperature Deviation

    Leica Biosystems Richmond Inc. is recalling 13 units of MSH6 antibody (REF PA0804) because a delay in transit may have caused the product to be stored outside of required temperature ranges.

    Product
    Cell Marque, MSH6 (44 Mab.), 7 mL, REF PA0804, IVD, The antibody is intended for in vitro diagnostic (IVD) use. MSH6 is a mismatch repair gene which is deficient in a high proportion of patients with microsatellite instability (MSI-H). This finding is associated with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1139-2017·2017-09-20

    VistaPharm Recalls Hydrocodone and Acetaminophen Oral Solution Due to Labeling Error

    VistaPharm, Inc. is recalling 3,084 bottles of Hydrocodone Bitartrate and Acetaminophen Oral Solution because the product was incorrectly labeled as a Class III controlled substance instead of a Class II controlled substance.

    Product
    Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771 ---- NDC 66689-023-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3128-2017·2017-09-20

    Fujifilm ED-530XT Endoscope Manuals Recalled Following FDA Inspection

    Fujifilm is recalling 260 user manuals for the ED-530XT endoscope following an FDA inspection. The recall is a corrective action to address documentation issues.

    Product
    Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V574000·2017-09-19

    Mercedes-Benz Recalls Four 2017 Models for Steering Defect

    Mercedes-Benz is recalling four 2017 vehicles due to improperly welded steering pins that may disable power assist, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, AMG E43, GLC300, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E051000·2017-09-17

    Curt Trailer Hitches Recalled for Mini Clubman and Countryman Models

    Curt Manufacturing is recalling Class 1 trailer hitches for 2016-2018 Mini Clubman and Countryman vehicles because the mounting points may be inadequate, causing the hitch to sag or separate.

    Product
    MINI — MINI COUNTRYMAN, CLUBMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V571000·2017-09-15

    Nissan Recalls 2017 Infiniti Q50 Vehicles for Air Bag Inflator Defect

    Nissan is recalling 2017 Infiniti Q50 and Q50 Hybrid vehicles because the driver's air bag inflator may be improperly welded, increasing injury risk in a crash.

    Product
    INFINITI — INFINITI Q50 HYBRID, Q50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·101-2017·2017-09-15

    Sausage Products Recalled for Undeclared Milk Allergen and Misbranding

    America New York RI Wang Food Group is recalling pork sausage products containing undeclared milk. The recall covers approximately 53,973 pounds distributed in New Jersey and New York.

    Product
    America New York RI Wang Food Group Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V573000·2017-09-15

    Forest River Recalls Vibe and Rainier Trailers for Propane Line Defect

    Forest River is recalling 2015-2018 Vibe and 2016-2018 Rainier recreational trailers because the liquid propane line may have insufficient clearance, posing a fire risk.

    Product
    FOREST RIVER — FOREST RIVER VIBE, RAINIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17224·2017-09-14

    Southwire Recalls Moonrays Globe Stake Lights Due to Fire Hazard

    Southwire is recalling Moonrays mystic globe and snow globe stake lights because light refraction can singe or melt nearby items, posing a fire hazard.

    Product
    Moonrays mystic globe and snow globe stake lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V569000·2017-09-14

    Mitsubishi Recalls Lancer Vehicles Due to Air Bag Inflator Rupture Risk

    Mitsubishi is recalling 2004-2006 Lancer and 2004 Lancer Sportback vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.

    Product
    MITSUBISHI — MITSUBISHI LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17C003000·2017-09-14

    Diono Recalls Multiple Convertible and Booster Car Seats for Crash Protection Defect

    Diono is recalling specific Radian, Olympia, Pacifica, and Rainier car seats manufactured between late 2013 and early 2017. The seats may not adequately protect children from chest injuries in crashes if installed forward-facing with only a lap belt.

    Product
    CHILD SEAT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide