The Recall Desk

State

Indiana product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50476–50500 of 83425

  • ModerateFDA (Devices)·Z-0985-2017·2017-01-18

    Bard Access Systems Recalls MiniLoc Safety Infusion Sets Due to Labeling Errors

    Bard Access Systems is recalling MiniLoc Safety Infusion Sets because some units have needle lengths and gauges that differ from the label descriptions.

    Product
    MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code: S02022-75. Packaged as single units in thermoformed trays. There are 20 MiniLoc¿ trays per case and 160 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1016-2017·2017-01-18

    Hospira Recalls Minibore Extension Sets Due to Solvent Occlusion

    Hospira is voluntarily recalling one lot of Minibore Extension Sets due to a confirmed report of solvent occlusion that may prevent priming and delay therapy.

    Product
    Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free Intended use: For the administration of drugs and solutions to a patient's vascular system through a vascular access device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0998-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall

    Siemens Medical Solutions is recalling Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Bio mCT-S(40) 3R->4R Upgrade, Material Number 10250743 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0973-2017·2017-01-18

    GE Healthcare Recalls OEC 9800 Imaging Systems Due to Power Cable Failures

    GE Healthcare is conducting a voluntary field action for OEC 9800 systems because the workstation power cable assembly can cause intermittent power cord failures.

    Product
    OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic…
    Category
    Medical Device
    Distribution
    50 states
  • ModerateUSDA FSIS·006-2017·2017-01-18

    Burgers Ozark Country Cured Recalls Mislabeled Turkey Products

    Burgers Ozark Country Cured is recalling approximately 1,905 pounds of fully cooked turkey products due to misbranding. The products contain undeclared sodium nitrite.

    Product
    Burger's Ozark Country Cured Hams, Inc. — Burgers Ozark Country Cured Recalls Poultry Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1091-2017·2017-01-18

    Piazza Produce Recalls Chili Powder for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling various sizes of chili powder because the product labeling does not contain a listing of ingredients.

    Product
    Chili Powder, 5 lb plastic gallon, product number 62235; Chili Powder, 1.25 lb plastic jar, product number 62216; Chili Powder, 10 lb plastic pail, product number 62254; Chili Powder, 22 lb plastic pail, product number 62273
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0986-2017·2017-01-18

    Bard Access Systems Recalls SafeStep Huber Needle Sets Due to Labeling Errors

    Bard Access Systems is recalling SafeStep Huber Needle Sets because some units may have needle lengths or gauges that differ from the label.

    Product
    SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as single units in thermoformed trays. There are 25 SafeStep¿ trays per case and 100 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood sampling through…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0996-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 102 Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(64)-4R, Material Number 10248672 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1000-2017·2017-01-18

    Siemens Biograph mCT 20 Excel PET/CT Scanner Recall for Laser Cover Windows

    Siemens is recalling 51 Biograph mCT 20 Excel scanners because laser cover windows may fall off.

    Product
    BIOGRAPH mCT 20 Excel, Material Number 10507786 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0955-2017·2017-01-18

    VOCO Futurabond M+ adhesive recalled for labeling mix-up

    Voco GmbH is recalling 50 units of VOCO Futurabond M+ adhesive due to a labeling error where the product was marked as Futurabond M+ Universal Adhesive.

    Product
    VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with methacrylate-based restorative, core build-up or luting materials. It can be applied with phosphoric acid etching (selective enamel etching or total-etch) of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0429-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0994-2017·2017-01-18

    Siemens Biograph mCT X-4R Laser Cover Window Recall

    Siemens is recalling 71 Biograph mCT X-4R scanners because laser cover windows may fall off.

    Product
    Biograph mCT X-4R, Material Number 10248670 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0983-2017·2017-01-18

    Bausch & Lomb Recalls Algerbrush-II Ophthalmic Surgical Instruments

    Bausch & Lomb is recalling Algerbrush-II surgical instruments because some units shipped with outdated operating instructions.

    Product
    Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0992-2017·2017-01-18

    Siemens Biograph mCT PET/CT Scanner Laser Cover Window Recall

    Siemens is recalling 41 Biograph mCT PET/CT scanners because laser cover windows may fall off.

    Product
    Biograph mCT S(40)-3R, Material Number 10248668 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1019-2017·2017-01-18

    Acumed Recalls OPT Croutons Synthetic Bone Substitute Due to Sterilization Documentation Issues

    Acumed LLC is recalling 83 units of OPT Croutons synthetic bone substitute because documentation for the sterilization dose was inadequate. The product was distributed in ten US states and Puerto Rico.

    Product
    OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium phosphate. The tricalcium phosphate is a soluble calcium phosphate salt.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0997-2017·2017-01-18

    Siemens Biograph mCT X-3R Scanners Recalled for Falling Laser Cover Windows

    Siemens Medical Solutions is recalling 18 Biograph mCT X-3R scanners because laser cover windows may fall off.

    Product
    Biograph mCT X-3R, Material Number 10248673 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1098-2017·2017-01-18

    Piazza Produce Recalls Hickory Smoke Salt for Missing Ingredient Labeling

    Piazza Produce is recalling 283 units of Hickory Smoke salt because the product labeling does not contain a listing of ingredients.

    Product
    Hickory Smoke salt, 7.5 lb plastic gallon, product number 64527; Hickory Smoke salt, 2.25 lb plastic jar, product number 64553; Hickory Smoke salt, 15 lb plastic pail, Product code 64591
    Category
    Food
    Distribution
    5 states
  • LowUSDA FSIS·007-2017·2017-01-18

    Willow Tree Poultry Farm Recalls Misbranded Chicken Salad Products

    Willow Tree Poultry Farm is recalling 204 pounds of chicken salad products because they are misbranded as chicken salad but contain egg salad.

    Product
    WILLOW TREE POULTRY FARM, INC. — Willow Tree Poultry Farm, Inc. Recalls Chicken Salad Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1096-2017·2017-01-18

    Piazza Produce Garlic Salt Recalled for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling various sizes of Garlic Salt because the product labeling does not contain a listing of ingredients.

    Product
    Garlic Salt, 9 lb plastic gallon, product number 64078; Garlic Salt, 2.5 lb plastic jar, product number 64059; Garlic Salt, 20 lb plastic pail, Product code 64097; Garlic Salt, 34 lb plastic pail, Product code 64116
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1103-2017·2017-01-18

    Piazza Produce Recalls Pumpkin Pie Spice for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling 197 units of pumpkin pie spice because the product labeling does not contain a listing of ingredients.

    Product
    Pumpkin pie spice, 4 lb plastic gallon, product number 67644; Pumpkin pie spice, 1 lb plastic jar, product number 67642
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1108-2017·2017-01-18

    Piazza Produce Recalls Taco Seasoning for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling 701 units of taco seasoning because the product labeling does not contain a listing of ingredients.

    Product
    Taco seasoning, 5.5 lb plastic gallon, product number 68667; Taco seasoning, 1.5 lb plastic jar, product number 68665
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1087-2017·2017-01-18

    Piazza Produce Recalls BBQ Spice for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling specific lots of BBQ Spice because the product labeling does not contain a listing of ingredients.

    Product
    BBQ Spice, 6 lb plastic gallon, product number 61608; BBQ Spice, 1.75 lb plastic jar, product number 61589; BBQ Spice, 15 lb plastic pail, product number 61627
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1088-2017·2017-01-18

    Piazza Produce Recalls Blackened Seasoning for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling 715 units of blackened seasoning because the product labels do not list ingredients. The recall covers food service establishments in five states.

    Product
    Blackened seasoning, 5.5 lb plastic gallon, product number 61703; Blackened seasoning, 1.5 lb plastic jar, product number 61684; Blackened seasoning, 10 lb plastic pail, product number 61722
    Category
    Food
    Distribution
    5 states
  • LowFDA (Food)·F-1090-2017·2017-01-18

    Piazza Produce Recalls Celery Salt for Missing Ingredient Labeling

    Piazza Produce, Inc. is recalling celery salt products because the packaging does not list ingredients. The recall affects food service establishments in five states.

    Product
    Celery salt, 8 lb plastic gallon, product number 62064; Celery salt, 2 lb plastic jar, product number 62045; Celery salt, 16 lb plastic pail, product number 62083
    Category
    Food
    Distribution
    5 states
  • LowFDA (Drugs)·D-0424-2017·2017-01-18

    Pfizer Recalls Cytotec Tablets Due to Failed Impurity Specifications

    Pfizer is recalling 1,706 cartons of Cytotec (misoprostol) tablets nationwide because the product failed impurity and degradation specifications.

    Product
    CYTOTEC — CYTOTEC (MISOPROSTOL)
    Category
    Drug
    Distribution
    Distributed nationwide