State

Indiana product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29051–29075 of 83188

SevereFDA (Drugs)·D-0227-2021·2021-01-20
Nostrum Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity
Nostrum Laboratories is recalling Metformin Hydrochloride Extended-Release Tablets, 750 mg, because the product contains N-Nitrosodimethylamine (NDMA) above acceptable intake levels.
Product
Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg, 100 tablets per bottle, Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120, NDC: 29033-056-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0852-2021·2021-01-20
Philips Emission Computed Tomography System Software Defect Recall
Philips is recalling 2,714 Emission Computed Tomography Systems due to a software defect that may cause image misdiagnosis and incorrect patient treatment.
Product
Emission Computed Tomography System Image Process System - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V016000·2021-01-20
RAM 4500 and 5500 Recalled for Rear Brake Line Wear Risk
Custom Truck And Body Works is recalling 2020 RAM 4500 and 5500 vehicles because a rear brake line may wear, causing brake failure.
Product
RAM — RAM 4500, 5500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0838-2021·2021-01-20
Fresenius Naturalyte Liquid Acid Concentrate Recalled for Conductivity Deviation
Fresenius Medical Care is recalling Naturalyte Liquid Acid concentrate bottles due to conductivity deviations and calcium concentration below manufacturing specifications.
Product
Naturalyte Liquid Acid concentrate bottles, Product Code 08-4231-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0656-2021·2021-01-20
Siemens Artis Medical Imaging Systems Recalled for Radiation Safety Defect
Siemens is recalling Artis zee, Artis Q, and Artis Pheno systems because the Air Kerma Rate can exceed regulatory limits when frame rates are increased during continuous release.
Product
Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0816-2021·2021-01-20
Fresenius NaturaLyte Liquid Acid Concentrate Recall for Low Sodium Levels
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Product
NaturaLyte Liquid Acid concentrate bottles, Model Number 08-2301-3 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V017000·2021-01-20
2021 Thomas Built Buses Recall for Brake Caliper Bolt Tightening Defect
Daimler Trucks North America is recalling 2021 Thomas Built Buses Saf-T-Liner HDX and EFX school buses because a brake caliper bolt may be incorrectly tightened, potentially reducing brake effectiveness.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0813-2021·2021-01-20
Fresenius Recalls NaturaLyte Liquid Acid Concentrate Bottles
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Product
NaturaLyte Liquid Acid concentrate bottles, Model Number 08-2201-5 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0831-2021·2021-01-20
Fresenius Naturalyte Liquid Acid concentrate bottles recalled for conductivity deviation
Fresenius Medical Care is recalling Naturalyte Liquid Acid concentrate bottles due to conductivity deviations and calcium concentration below specification.
Product
Naturalyte Liquid Acid concentrate bottles, Product Code 08-1251-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0734-2021·2021-01-20
Boston Scientific Recalls Lotus Edge Valve Systems Due to Deployment Failure Risk
Boston Scientific is recalling 207 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Product
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF H749LVS230, GTIN 08714729940814, Made in Ireland, Ballybrit Business Park, Galway, Ireland.
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-0728-2021·2021-01-20
Boston Scientific Recalls Lotus Edge Valve Systems Due to Deployment Failure Risk
Boston Scientific is recalling 219 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Product
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF H749LVSUS230, GTIN 08714729960904
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-0735-2021·2021-01-20
Recall of Lotus Edge Valve System Transcatheter Aortic Valve Prosthesis Due to Deployment Locking Failure
Boston Scientific recalls 278 Lotus Edge Valve Systems due to a failure in visual inspection that prevents proper valve locking during deployment, potentially preventing delivery system release.
Product
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 25mm, sterile, REF H749LVS250, GTIN 08714729940821, Made in Ireland, Ballybrit Business Park, Galway, Ireland.
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-0828-2021·2021-01-20
Fresenius Citrasate Liquid Acid Concentrate Recall Due to Low Sodium Levels
Fresenius Medical Care is recalling 198 drums of Citrasate Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.
Product
Citrasate Liquid Acid concentrate drums, Model Number 13-2251-CA - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0841-2021·2021-01-20
Fresenius Citrasate Liquid Acid concentrate drums recalled for conductivity deviation
Fresenius Medical Care is recalling two drums of Citrasate Liquid Acid concentrate due to deviations in sodium conductivity and calcium concentration.
Product
Citrasate Liquid Acid concentrate drums, Product Code 13-2251 -CA - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0834-2021·2021-01-20
Fresenius Citrasate Liquid Acid Concentrate Recalled for Conductivity Deviation
Fresenius Medical Care is recalling Citrasate Liquid Acid concentrate bottles due to conductivity deviations and low calcium levels.
Product
Citrasate Liquid Acid concentrate bottles, Product Code 08-2251-CA - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0837-2021·2021-01-20
Fresenius Naturalyte Liquid Acid concentrate bottles recalled for conductivity deviation
Fresenius Medical Care is recalling Naturalyte Liquid Acid concentrate bottles due to deviations in conductivity and calcium concentration.
Product
Naturalyte Liquid Acid concentrate bottles, Product Code 08-3251-9 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0817-2021·2021-01-20
Fresenius NaturaLyte Liquid Acid Concentrate Recall for Low Sodium Levels
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Product
NaturaLyte Liquid Acid concentrate bottles, Model Number 08-2351-8 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0861-2021·2021-01-20
Siemens Atellica CH 930 Analyzer Software Recall for Discrepant Results
Siemens Healthcare Diagnostics is recalling Atellica CH 930 Analyzers with software version 1.23.2 or lower because multiple software issues may lead to the reporting of discrepant patient results.
Product
Atellica CH 930 Analyzer - In vitro diagnostic testing of clinical specimens. Product Siemens Material Number (SMN): 11067000 - Product Usage: intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric, chemiluminescent, and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0836-2021·2021-01-20
Fresenius Naturalyte Liquid Acid Concentrate Recall for Conductivity Deviation
Fresenius Medical Care is recalling 123 bottles of Naturalyte Liquid Acid concentrate due to conductivity deviations and low calcium levels.
Product
Naturalyte Liquid Acid concentrate bottles, Product Code 08-2351-8 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0859-2021·2021-01-20
ICU Medical Cogent Hemodynamic Monitoring System Recalled for Software Issue
ICU Medical is recalling 220 Cogent Hemodynamic Monitoring Systems because a software issue may cause the display to show incorrect continuous cardiac output values after calibration.
Product
icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the monitoring of continuous cardiac output and calculated hemodynamic parameters is indicated for diagnostic and prognostic evaluation by a clinician.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0815-2021·2021-01-20
Fresenius NaturaLyte Liquid Acid Concentrate Recall for Low Sodium Levels
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Product
NaturaLyte Liquid Acid concentrate bottles, Model Number 08-2251-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0811-2021·2021-01-20
Fresenius NaturaLyte Liquid Acid Concentrate Recall for Low Sodium Levels
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Product
NaturaLyte Liquid Acid concentrate bottles, Model Number 08-1251-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0823-2021·2021-01-20
Fresenius NaturaLyte Liquid Acid Concentrate Recall for Low Sodium Levels
Fresenius Medical Care is recalling 51 drums of NaturaLyte Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.
Product
NaturaLyte Liquid Acid concentrate drums, Model Number 13-1251-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0863-2021·2021-01-20
Siemens Atellica IM 1600 Analyzer Software Recall for Discrepant Results
Siemens Healthcare Diagnostics is recalling Atellica IM 1600 Analyzers with software version 1.23.2 or lower because multiple software issues may lead to the reporting of discrepant patient results.
Product
Atellica IM 1600 Analyzer - In vitro diagnostic testing of clinical specimens. Product Siemens Material Number (SMN): 11066000 - Product Usage: intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric, chemiluminescent, and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0843-2021·2021-01-20
Medtronic CareLink Diabetes Software Recalled for Data Transfer Errors
Medtronic is recalling CareLink Personal and System software due to potential RF interference during data uploads, which may cause incomplete basal rate information and inappropriate therapy changes.
Product
CareLink Personal Software Therapy Management Software Tool for Diabetes CareLink System Therapy Management Software Tool for Diabetes Software Uploader versions: 3.1.5.000 3.1.2.000
Category
Medical Device
Distribution
Distributed nationwide