State

Indiana product recalls

73,100 recalls have nationwide distribution and so reach Indiana. 9,585 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,585
Critical: 1,913
Severe: 2,148
Most recent: 2026-09-23

Of the 9,585 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,148 (22%) are Severe.

Which agencies issued them

These figures cover only the 9,585 recalls whose distribution notice names Indiana specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11626–11650 of 82685

SevereFDA (Food)·F-1365-2024·2024-06-19
Grande Bravo Whey Protein Recalled Due to Salmonella Contamination
Grande Bravo 550 Functional Whey Protein is being recalled due to possible Salmonella contamination. Affected batches ANV508-1 and ANV508-3 were distributed across 24 U.S. states and internationally.
Product
Grande Bravo 550 Functional Whey Protein SKU 32105. 34% Protein. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1354-2024·2024-06-19
Seasoning Ingredient Recalled for Potential Salmonella Contamination
Kerry, Inc is recalling BrS8 RODIZIO Seas No MSG seasoning ingredient due to potential Salmonella contamination. The affected product was distributed to multiple U.S. states and Canada.
Product
BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
Category
Food
Distribution
8 states
SevereFDA (Food)·F-1357-2024·2024-06-19
Kerry Cheddar and Sour Cream Seasoning Recall for Potential Salmonella
Kerry Inc. is recalling 77 bags of Cheddar & Sour Cream SEAS seasoning (lots 8092105, 8127605, 8091886) distributed across multiple U.S. states and Canada due to potential Salmonella contamination.
Product
Cheddar & Sour Cream SEAS 22.68kg. Net Weight: 50.00 lb (22.68 kg) SAP Code: 20651520. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
Category
Food
Distribution
8 states
SevereFDA (Food)·F-1363-2024·2024-06-19
Grande Bravo 300 Whey Protein Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Bravo 300 Functional Whey Protein (SKU 32102) due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
Product
Grande Bravo 300 Functional Whey Protein SKU 32102. 34% Protein. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1347-2024·2024-06-19
Mt. Capra Goat Milk Formula Kit Recalled for Lack of FDA Premarket Notification
Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.
Product
Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.) and Bundle Refill. Each Goat Milk Formula Recipe Kit consist of 10 individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee -Extra Virgin Olive Oil -Expeller-Pressed Grapeseed Oil
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1367-2024·2024-06-19
FDA Recalls Grande Ultra Whey Protein Isolate for Possible Salmonella
GRANDE CHEESE COMPANY is recalling Grande Ultra 9100 Functional Whey Protein Isolate (SKU 32131) due to possible Salmonella contamination. The recall affects 1.7 million pounds distributed to 24 U.S. states and international markets.
Product
Grande Ultra 9100 Functional Whey Protein Isolate. SKU 32131. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1369-2024·2024-06-19
Whey Protein Isolate Recalled Due to Possible Salmonella Contamination
Grande Ultra 9150 Whey Protein Isolate (Product Code 32324) is being recalled due to possible Salmonella contamination. The affected product was distributed to 24 US states and internationally to Canada, Ecuador, and Japan.
Product
Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Protein. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Isolate Contains Milk. Manufactured By: Grande Custom Ingredients Group, 1007 West Lake Street, Friendship, WI 53934.
Category
Food
Distribution
24 states
SevereFDA (Devices)·Z-1921-2024·2024-06-19
Thoratec HeartMate System Monitor display malfunction in left ventricular assist devices
The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.
Product
Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L1286C, L1386, 1286A-CAN, 1286INT and L1286INT. Left ventricular assist device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0553-2024·2024-06-19
Docetaxel Injection Recalled Due to Particulate Matter in Stopper
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.
Product
DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1362-2024·2024-06-19
Grande Bravo Whey Protein Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Bravo 250 Functional Whey Protein (SKU 32101) for possible Salmonella contamination. The recall affects 1,726,910 pounds distributed across 24 U.S. states and exported to Canada, Ecuador, and Japan.
Product
Grande Bravo 250 Functional Whey Protein SKU 32101. Grade A. Pasteurized. Net Wt 50 lbs. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
SevereFDA (Food)·F-1368-2024·2024-06-19
Whey Protein Isolate Recalled for Possible Salmonella Contamination
Grande Cheese Company is recalling Grande Ultra 8000 Nutritional Whey Protein Isolate due to possible Salmonella contamination. The affected batches include AOE813-1 through AOE813-4 and AOF840-1 through AOF840-4.
Product
Grande Ultra 8000 Nutritional Whey Protein Isolate. SKU 32200. 80% Protein Dry Basis. Grade A. Pasteurized. Net Wt 20 kg. Ingredients: Whey Protein Concentrate Contains Milk. Grande Custom Ingredients Group, 250 Camelot Drive, Fond du Lac, WI
Category
Food
Distribution
24 states
HighFDA (Drugs)·D-0547-2024·2024-06-19
Klarity-C Ophthalmic Emulsion Recalled Due to Sterility Assurance Risk
Imprimis is recalling Klarity-C, a cyclosporine eye medication, because the company cannot assure the product meets sterility standards. Approximately 136,005 units were distributed nationwide.
Product
Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1% 5.5mL, Rx Only, This is a compounded drug. NOT FOR RESALE. OFFICE USE ONLY Compounded by: Imprimis NJOF, LLC., 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852 NDC: 71384-514-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2034-2024·2024-06-19
Streptococcal A Rapid Test Kits Recalled for Unauthorized At-Home Distribution
Wondfo USA has recalled Streptococcal A rapid test kits that are being sold for unauthorized at-home and direct-to-consumer use. The kits should not be used outside professional healthcare settings.
Product
Streptococcal A rapid test kits, labeled as: Wondfo Biotech Co., Ltd, WondView Strep A Test Kit, Guangzhou Wondfo Biotech Co., Ltd, Wondfo One Step Strep A Swab Test, Dealmed Medical Supplies LLC, Strep A Rapid Test Kit, Jant Pharmacal Corporation, Accustrip VALUPAK Strep A Test
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2041-2024·2024-06-19
MRI Systems Power Cable Terminal Block Fire Hazard Recall
Canon Medical MRI systems are being recalled because the terminal block securing the power cable may disconnect, potentially causing electrical arcing and fire. 153 units are affected across the United States and Puerto Rico.
Product
MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504), Vantage Titan 3T MRT-3010 (MEXL-3010), Vantage Galan 3T MRT-3020 (MEXL-3020)
Category
Medical Device
Distribution
38 states
HighFDA (Drugs)·D-0545-2024·2024-06-19
Prescription Drug Recall: Phenazopyridine Tablets Contain Wrong Medication
Winder Laboratories is recalling Phenazopyridine HCl tablets (Lot #1142404) due to a product mix-up where some bottles contain Phenobarbital tablets instead. No illnesses or injuries have been reported.
Product
PHENAZOPYRIDINE HYDROCHLORIDE — PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2033-2024·2024-06-19
Streptococcal A Rapid Test Kits Recalled for Unauthorized Distribution
Wondfo USA is recalling 102,500 units of IMCO Strep A Rapid Test Kits due to unauthorized distribution for at-home, over-the-counter, and direct-to-consumer use.
Product
Independent Medical Co-op Inc., Streptococcal A rapid test kits, labeled as: IMCO Strep A Rapid Test Strip and IMCO Strep A Rapid Test, Part Number STP25-IMC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2031-2024·2024-06-19
Streptococcal A Rapid Test Kits Recalled for Unauthorized Distribution
Wondfo USA has recalled 170,000 units of Clarity Strep A Rapid Test kits due to unauthorized distribution for at-home use, non-prescription use, over-the-counter use, and direct-to-consumer sales. The recall affects test kits distributed nationwide.
Product
Clarity and Clarity Diagnostics LLC, Streptococcal A rapid test kits, Labeled as: a) Clarity Strep A Rapid Test, Part Number CD-STP25, b) Clarity Diagnostics LLC, Clarity Strep A Rapid Test, Part Number CD-STP25V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2135-2024·2024-06-19
CORI Surgical System Software Error Causes Tracking Array Flickering
The CORI Starter Kit surgical system may experience display flickering from a software tracking error, potentially causing surgical delays during orthopedic procedures.
Product
CORI Starter Kit, Real Intelligence CORI, CORI STARTER KIT - UNIVERSAL.Intended to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures Product Numbers: (1) ROB10000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2129-2024·2024-06-19
OMTech Desktop Laser Engraver recalled for missing safety interlocks
Rygel Advanced Machines recalls OMTech Desktop Laser Engravers due to missing safety interlocks and labeling. The devices lack required redundant interlocks and certification labels that prevent accidental laser exposure.
Product
OMTech Desktop Laser Engraver
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2142-2024·2024-06-19
VITROS Immunodiagnostic Calibrators Recalled for Potential Accuracy Bias
Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.
Product
VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled Calibrator tube (1 per level: C1 - green, C2 - yellow, C3 - red).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2139-2024·2024-06-19
Aeos Robotic Digital Microscope recalled for safety mechanism failure
Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.
Product
Aeos Robotic Digital Microscope, Product Code: PV010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2138-2024·2024-06-19
EVD Catheter Sterile Packaging Defect Recall for Intracranial Drainage
Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.
Product
CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2136-2024·2024-06-19
CODMAN BACTISEAL EVD Catheter Set: Sterile packaging defect recalled
Integra LifeSciences is recalling 135 CODMAN BACTISEAL EVD Catheter Sets due to defects in sterile packaging that may compromise product sterility.
Product
CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial p
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V455000·2024-06-19
2020–2025 Porsche Taycan front brake hoses can crack
Porsche is recalling certain 2020–2025 Taycan vehicles because the front brake hoses can develop cracks and leak brake fluid, reducing braking performance. Dealers will replace the hoses for free.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0548-2024·2024-06-19
FDA Recalls Eye Suspension Medication for Lack of Sterility Assurance
Imprimis NJOF, LLC is recalling one lot of a compounded ophthalmic suspension due to failure of sterility assurance. The product may be contaminated and pose a risk of serious eye infection.
Product
Prednisolone-Moxifloxacin-Bromfenac Sterile Ophthalmic Suspension, 1%, 0.5%, 0.075%, 5mL, Quantity: 20mL, Rx Only, Compounded by: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ NDC 71384-310-05
Category
Drug
Distribution
Distributed nationwide