State

Indiana product recalls

73,509 recalls have nationwide distribution and so reach Indiana. 9,590 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,590
Critical: 1,913
Severe: 2,529
Most recent: 2026-10-24

Of the 9,590 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 2,529 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,590 recalls whose distribution notice names Indiana specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26201–26225 of 83099

SevereFDA (Drugs)·D-0783-2021·2021-09-08
MEDICALLY MINDED Hand Sanitizer Gel Recalled for Manufacturing Deviations
Global Sanitizers LLC is recalling MEDICALLY MINDED Hand Sanitizer Gel (70% ethyl alcohol, 8 fl oz bottles) distributed nationwide due to manufacturing deviations under conditions that produced a methanol-contaminated product lot.
Product
MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8 Fl OZ (236 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200. Distributed by SBL Brands, LLC Las Vegas, NV 89119 UPC: 6…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0902-2021·2021-09-08
Cahill Whiskey Cheddar Cheese Recalled for Potential Listeria Contamination
Whole Foods Market is recalling Cahill Whiskey Cheddar Cheese due to potential contamination with Listeria monocytogenes. The cheese was distributed to stores across multiple states from May to July 2021.
Product
Cahill Whiskey Cheddar Cheese packaged in clear plastic PLU 5478494884
Category
Food
Distribution
22 states
SevereFDA (Food)·F-0892-2021·2021-09-08
BrightFarms Lakeside Crunch Salad Recalled for Potential Salmonella Contamination
BrightFarms Lakeside Crunch salad, sold in 4oz packages, is being recalled due to potential Salmonella contamination. The product was distributed across Illinois, Wisconsin, Iowa, Indiana, and Michigan.
Product
BrightFarms Lakeside Crunch; packaged in clear, plastic clamshell; 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0897-2021·2021-09-08
BrightFarms Spinach Recall Due to Potential Salmonella Contamination
BrightFarms Spinach packaged in 4oz and 8oz clamshells may be contaminated with Salmonella. The affected product was grown at the company's Rochelle, Illinois indoor farm and distributed across multiple Midwest states.
Product
BrightFarms Spinach; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0890-2021·2021-09-08
BrightFarms Harvest Crunch Salmonella Contamination Recall
BrightFarms Harvest Crunch packaged salad may be contaminated with Salmonella. The recall affects products distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms Harvest Crunch; packaged in clear plastic clamshells; 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Drugs)·D-0779-2021·2021-09-08
MEDICALLY MINDED Hand Sanitizer Gel Recalled for Methanol Contamination
Global Sanitizers LLC is recalling MEDICALLY MINDED Hand Sanitizer Gel (8.5 FL OZ) due to potential methanol contamination. The product was manufactured under the same conditions as a lot previously found to contain methanol.
Product
MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ (250 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119.…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0782-2021·2021-09-08
MEDICALLY MINDED Hand Sanitizer Gel Recalled for Methanol Contamination
Global Sanitizers LLC is recalling MEDICALLY MINDED Hand Sanitizer Gel (Ethyl Alcohol 70% v/v, 8.5 FL OZ / 250 mL) distributed nationwide due to manufacturing conditions that led to methanol contamination in product lots.
Product
MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1 ,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0778-2021·2021-09-08
Hand Sanitizer Gel Recalled Due to Methanol Contamination Risk
Global Sanitizers LLC is recalling MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel (70% ethyl alcohol) due to manufacturing deviations. Products were made under the same conditions as a lot found to contain methanol.
Product
MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera, (Ethyl Alcohol 70% v/v), 10 FL OZ / 300 mL, Manufactured by Grupo V-Klean S.A. de C.V, Calle Alborada 124, Parques del Pedregal, Tlalpan, 14250 Ciudad de Mexico, CDMX, Distributed by SBL Brands, LLC. Las Vegas, NV…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0901-2021·2021-09-08
Cahill Cheddar with Porter Cheese Recalled for Listeria Contamination Risk
Whole Foods Market is recalling Cahill Cheddar with Porter cheese (PLU 93579) sold in clear plastic packaging due to potential contamination with Listeria monocytogenes, a serious foodborne pathogen.
Product
Cahill Cheddar with Porter PLU 93579 packaged in clear plastic
Category
Food
Distribution
22 states
SevereFDA (Food)·F-0896-2021·2021-09-08
BrightFarms Mighty Romaine Recalled for Potential Salmonella Contamination
BrightFarms is recalling Mighty Romaine lettuce sold in 4oz and 8oz clamshells because the product may be contaminated with Salmonella.
Product
BrightFarms Mighty Romaine; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
SevereFDA (Food)·F-0891-2021·2021-09-08
BrightFarms 50/50 Spring & Spinach Salmonella Contamination Recall
BrightFarms 50/50 Spring & Spinach in 4oz clamshells may be contaminated with Salmonella. The product was distributed in Illinois, Wisconsin, Iowa, Indiana, and Michigan with best-by dates through July 29, 2021.
Product
BrightFarms 50/50 Spring & Spinach; packaged in clear plastic clamshells, 4oz; grown at the company's Rochelle, Illinois indoor farm
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-2399-2021·2021-09-08
DePuy TruMatch CT Cut Guide Kit Recalled for Software Alignment Error
DePuy's TruMatch CT Cut Guide Kit is being recalled due to a software coding error that may cause misalignment of preoperative surgical positioning scans, potentially resulting in improper limb alignment during joint replacement surgery.
Product
TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number…
Category
Medical Device
Distribution
10 states
HighFDA (Devices)·Z-2395-2021·2021-09-08
Surgical instrument software error may cause limb misalignment
DePuy Orthopaedics' TruMatch CT Pin Guide Kit has a software coding error that may misalign bone landmarks during joint replacement surgery, potentially causing limb malalignment. No injuries have been reported.
Product
TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number…
Category
Medical Device
Distribution
10 states
HighFDA (Devices)·Z-2410-2021·2021-09-08
COVID-19/Flu Rapid Test Distributed to Non-Certified Laboratories
COVID-19/Flu rapid diagnostic test was distributed to laboratories not certified under federal clinical standards. The 563,290-unit recall affects nationwide distribution; products were authorized only for CLIA-certified laboratories.
Product
Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential Diagnosis of SARS-CoV-2, Influenzas Type A, and Type B Antigens Simultaneous qualitative detection and differentiation of nucleocapsid antigen from SARS-CoV-2, influenza A and influenza B directly from…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0904-2021·2021-09-08
Your Way Fresh Yogurt Parfait Recalled for Undeclared Soy
Your Way Fresh Sliced Banana + Strawberry Yogurt Parfait is being recalled because the yogurt ingredient contains soy lecithin, but soy is not declared on the product label. Consumers with soy allergies may face serious health risks.
Product
Your Way Fresh, Sliced Banana + Strawberry Yogurt Parfait; Net wt. 6.25 oz (177 g); UPC 8 54426 00807 8; Distributed by Your Way Fresh, Newport Beach, CA, 12 cups per case;
Category
Food
Distribution
7 states
HighFDA (Food)·F-1016-2021·2021-09-08
Rocky Top Farms Cherry Butter recalled for undeclared milk allergen
Rocky Top Farms Cherry Butter is being recalled because it contains undeclared milk, which can pose a serious risk to consumers with milk allergies. The recall affects retail and food service packages.
Product
Rocky Top Farms Cherry Butter sold in 1 gallon food service and 10oz retail sizes. 10 oz retail units may be sold individually and as multi-pack and variety packs online.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0776-2021·2021-09-08
Cyclobenzaprine Hydrochloride Tablets 7.5mg Recalled for Microbial Contamination
Teva Pharmaceuticals USA is recalling Cyclobenzaprine Hydrochloride Tablets 7.5mg (4,992 bottles, batch 1408824A, expiration 08/2023) distributed nationwide due to out-of-specification microbial test results in an excipient ingredient.
Product
Cyclobenzaprine Hydrochloride Tablets, 7.5mg, 100 count tablets per bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314, NDC 57237-266-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2378-2021·2021-09-08
Baxter PrismaFlex Dialysis Tubing Sets Recalled Due to Sterilization Failure
Baxter PrismaFlex dialysis tubing sets are being recalled because products labeled sterile may not have been properly sterilized due to sterilization contractor failures and data integrity issues.
Product
Baxter PrismaFlex, REF numbers: a) 106696 (M 60 SET) b) 106697 (M 100 SET) Expansion: c) 107144 (TPE2000 SET) d) 115307 (M 150 SET) e) 115309 (ST 100 SET) f) 955467 (M 150 SET) g) 955468 (ST 100 SET) h) 955595 (M 100 SET) i) 955596 (ST 150 SET) Used with…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2357-2021·2021-09-08
Medical Imaging Software Bug May Cause Incorrect X-ray Exposure
Philips CombiDiagnost R90 imaging software has a bug where exposure settings may change unexpectedly, resulting in over or under-exposed X-ray images. About 66 systems in the US are affected.
Product
CombiDiagnost R90 Software Version R1.0 and R1.1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2381-2021·2021-09-08
COVID-19 Antibody Test Kit Recalled for Failing Validation Requirements
Thera Test Laboratories is recalling 11 EL-Anti-SARS-CoV-2 IgM test kits distributed across six states because they failed to meet FDA's updated validation requirements for accurately detecting COVID-19 antibodies.
Product
EL-Anti-SARS-CoV-2 IgM Kit, Catalog #104-129, IVD. Submitted as EUA202129
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2394-2021·2021-09-08
CT Pin Guide Instruments Recalled for Software Imaging Alignment Error
The TruMatch CT Pin Guide Kit is being recalled due to a software error that may misalign surgical guidance images, potentially affecting limb positioning during hip, knee, and ankle surgery. No injuries have been reported.
Product
TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part…
Category
Medical Device
Distribution
10 states
HighFDA (Devices)·Z-2385-2021·2021-09-08
Diamondback 360 Gen2 Orbital Atherectomy System Crown Size Mislabeling Recall
Cardiovascular Systems Inc. is recalling 8 units of the Diamondback 360 Gen2 Peripheral Orbital Atherectomy System due to potential mislabeling of crown sizes. Units packaged as 1.50mm Solid Crown may actually be 1.25mm Micro Crown and vice versa.
Product
DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.5MM SOLID, 145 CM, REF DBP-150SOLID145
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0958-2021·2021-09-08
Hostess Soft White Hot Dog Buns Recalled for Listeria and Salmonella Risk
Hostess Brands is recalling Soft White Hot Dog Buns due to positive environmental samples for Listeria and Salmonella found by the contract manufacturer. The product was distributed to retailers and distributors across 34 U.S. states.
Product
Hostess Soft White Hot Dog Buns, Net Wt. 12 OZ, UPC 888109110970
Category
Food
Distribution
35 states
HighFDA (Devices)·Z-2396-2021·2021-09-08
Surgical alignment software error recalled in patient-specific orthopedic instruments
DePuy Orthopaedics recalls TruMatch surgical instruments due to a software error in the scanning alignment tool that may cause incorrect limb positioning during surgery.
Product
TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number…
Category
Medical Device
Distribution
10 states
HighFDA (Devices)·Z-2389-2021·2021-09-08
Marco Shoulder Stabilization Kit Recall Due to Sterilization Failure
Aspen Surgical Products is recalling 4,270 Marco Shoulder Stabilization Kits manufactured between July 2019 and July 2021 due to bioburden levels exceeding sterilization validation limits, which may compromise sterile fields and increase infection risk.
Product
Marco Shoulder Stabilization Kit, Product Code 711100, (previous product code 100601), Sample Kit S711100
Category
Medical Device
Distribution
Distributed nationwide