State

Indiana product recalls

73,363 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,587
Critical: 1,913
Severe: 2,149
Most recent: 2026-09-30

Of the 9,587 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 2,149 (22%) are Severe.

Which agencies issued them

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19101–19125 of 82950

HighFDA (Drugs)·D-0132-2023·2023-01-25
FDA Recalls Akorn AK-POLY-BAC Eye Ointment for CGMP Violations
Akorn Inc. voluntarily recalls 36,025 tubes of AK-POLY-BAC Bacitracin/Polymixin B eye ointment nationwide due to manufacturing process deviations affecting product quality and sterility.
Product
AK-POLY-BAC brand of Bacitracin cand Polymixin B Sulfate Ophthalmic Ointment USP, 3.5 g (1/8 oz.) tube, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-238-35
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0128-2023·2023-01-25
Prescription Anesthetic Drug Recalled for Subpotent Epinephrine Content
Fresenius Kabi is recalling Sensorcaine anesthetic injections nationwide due to subpotent epinephrine content. Affected batches may not provide adequate anesthesia or hemostasis during procedures.
Product
SENSORCAINE — SENSORCAINE (BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0956-2023·2023-01-25
ARTIS medical imaging systems recalled for mechanical connection failure
Siemens ARTIS pheno and ARTIS icono imaging systems are recalled because the mechanical connection between the tabletop and table base may fail. The recall affects 550 units distributed worldwide.
Product
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V028000·2023-01-25
2022 Hyundai Santa Fe Plug-In Hybrid fuel tank defect recall
Hyundai is recalling certain 2022 Santa Fe Plug-In Hybrid vehicles due to improperly molded fuel tanks that may leak gasoline. A fuel leak in the presence of an ignition source can increase the risk of fire.
Product
HYUNDAI — HYUNDAI SANTA FE PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0998-2023·2023-01-25
FDA Recalls Thoracic Stent-Graft Systems Over Manufacturing Size Defect
Bolton Medical has recalled 640 units of RELAY PRO thoracic stent-graft systems worldwide because the products may be shorter than their packaging indicates.
Product
RELAY PRO, THORACIC STENT-GRAFT SYSTEM, REF 28-N4-XX-XXX-XXX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0264-2023·2023-01-25
Klosterman 100% Whole Wheat Breads Recalled for Insanitary Conditions
Klosterman Baking Company is recalling 100% whole wheat breads distributed in Indiana, Ohio, and Tennessee due to products being held under insanitary conditions. Affected breads were delivered between December 12-16, 2022.
Product
Breads: 100% whole wheat product 1415 Klosterman Retail UPC # 0005172100367 Loaf 1 12 oz. 100% whole wheat product 1448 Klosterman Retail UPC # 0005172100401 Loaf 1 24 oz.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0984-2023·2023-01-25
Cardinal Health Jackson-Pratt Channel Drains recalled for multiple performance defects
Cardinal Health is recalling 2,277 Jackson-Pratt Channel Drains due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. These defects may affect the drain's function and clinical performance.
Product
Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2226
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0273-2023·2023-01-25
French Bread Products Recalled for Insanitary Holding Conditions
Klosterman Baking Company is recalling French bread products (16 oz. loaves, SKUs 8510, 8550, 8551) distributed in Indiana, Ohio, and Tennessee because they were held under insanitary conditions.
Product
Breads: Frenchbread product 8510 Clear Bag Loaf 1 16 oz. Frenchbread product 8550 Clear Bag Loaf 1 16 oz. Frenchbread product 8551 Clear Bag Loaf 6 16 oz.
Category
Food
Distribution
3 states
HighFDA (Food)·F-0288-2023·2023-01-25
Klosterman whole grain breads recalled for insanitary storage conditions
Klosterman Baking Company is recalling 109,343 units of whole grain breads and baked goods sold in Indiana, Ohio, and Tennessee that were held under insanitary conditions. Products were delivered between December 12-16, 2022.
Product
Breads: Whole grain product 1290 Clear Bag Loaf 1 24 oz. Whole grain product 1292 Clear Bag Loaf 1 24 oz. Whole grain product 3474 Clear Bag Buns 12 60 g Whole grain product 3478 Clear Film Buns 60 60 g Whole grain product 3709 Clear Bag Buns 12 1.75 oz. Whole grain…
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0994-2023·2023-01-25
Cardinal Health Jackson-Pratt Surgical Drains Recalled for Multiple Defects
Cardinal Health recalls Jackson-Pratt Channel Drains due to reported defects including non-visibility on imaging, dull insertion trocars, reduced flexibility, and broken drain tips.
Product
Cardinal Health Jackson-Pratt Channel Drain, 32 Fr, REF JP-2292
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0980-2023·2023-01-25
Cardinal Health Jackson-Pratt Channel Drains Recalled for Multiple Performance Defects
Cardinal Health is recalling 750 units of Jackson-Pratt Channel Drains (10 mm) due to multiple performance issues including broken drain tips, lack of radiopacity, dull trocars, and reduced flexibility that could affect surgical outcomes.
Product
Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2217
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0969-2023·2023-01-25
Cardinal Health Jackson-Pratt Channel Drain: Multiple Performance Defects
Cardinal Health is recalling Jackson-Pratt Channel Drains due to multiple reported performance defects including dull trocars, lack of flexibility, missing radiopacity, and broken tips. These issues may compromise insertion and drain function.
Product
Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2188
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0976-2023·2023-01-25
Cardinal Health Jackson-Pratt Channel Drains Recalled for Multiple Performance Defects
Cardinal Health Jackson-Pratt Channel Drains are recalled for performance defects including dull trocars, broken tips, lack of flexibility, and lack of radiopacity. 220 units are affected.
Product
Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2213
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0995-2023·2023-01-25
Vasoshield Syringe Ink Chips May Cause Embolic Events
Ink on the Vasoshield syringe may chip off, potentially causing blood clots and foreign body reactions in patients. About 9,817 devices are affected.
Product
Hemopro 2 with Vasoshield, Model VH-4001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0304-2023·2023-01-25
Superior Fresh Spring Mix Recalled for Glass Particle Contamination
Superior Fresh is recalling Spring Mix lettuce products that may contain small glass particles. The affected packages were distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.
Product
Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Butter lettuce, Arugula, spinach. Keep Refrigerated. Packaged under the following Names and sizes: 1. Spring Mix Family Pack Net Wt. 8 oz…
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0986-2023·2023-01-25
Cardinal Health Jackson-Pratt Drain Recalled for Performance Defects
Cardinal Health is recalling Jackson-Pratt Channel Drains (15 Fr, REF JP-2228) due to multiple performance issues including dull trocars, broken wound tips, lack of radiopacity, and inflexibility. The recall affects approximately 15,493 units distributed worldwide.
Product
Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2228
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2023·2023-01-25
Cardinal Health Jackson-Pratt Channel Drain recalled for performance defects
Cardinal Health is recalling Jackson-Pratt Channel Drains (10 mm, model JP-2212) due to multiple performance defects including lack of radiopacity, dull trocars, reduced flexibility, and broken wound tips.
Product
Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2212
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0153-2023·2023-01-25
Proparacaine Ophthalmic Solution Recalled for Manufacturing Quality Deviations
Akorn is voluntarily recalling Proparacaine Ophthalmic Solution nationwide due to Current Good Manufacturing Practice deviations.
Product
Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5%, 15 mL per dropper bottle, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031 NDC: 17478-263-12
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0279-2023·2023-01-25
Klosterman Baking Company onion buns and bread recalled for insanitary storage
Klosterman Baking Company is recalling onion buns and bread distributed in Indiana, Ohio, and Tennessee for products held under insanitary conditions. Consumers should discard affected items.
Product
Breads: Onion product 3655 Clear Film Buns 20 69 g
Category
Food
Distribution
3 states
HighNHTSA·23V027000·2023-01-25
2022 Kia Sorento PHEV fuel tank defect fire risk
Kia is recalling certain 2022 Sorento Plug-In Hybrid vehicles due to improperly molded fuel tanks that may leak. A fuel leak near an ignition source could increase the risk of fire.
Product
KIA — KIA SORENTO PHEV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0165-2023·2023-01-25
Prescription Rifampin Capsules Recalled Due to Failed Quality Specifications
Amerisource Health Services is recalling Rifampin Capsules USP 300 mg nationwide due to failed impurities and degradation specifications. Affected patients should contact their healthcare provider before using remaining inventory.
Product
RIFAMPIN — RIFAMPIN (RIFAMPIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0286-2023·2023-01-25
Klosterman Wheat Bread Loaves Recalled for Insanitary Storage Conditions
Klosterman Baking Company is recalling approximately 109,343 wheat bread loaves distributed in Indiana, Ohio, and Tennessee that were held under insanitary conditions, creating a potential contamination risk.
Product
Breads: Wheat product 1305 Klosterman Foodservice UPC # 0005172100452 Loaf 1 28 oz. Wheat product 1306 Clear Bag Loaf 1 32 oz. Wheat product 1310 Clear Bag Loaf 1 24 oz. Wheat product 1358 Klosterman Retail UPC # 0005172100714 Loaf 1 24 oz. Wheat product 1380 Pennington…
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0985-2023·2023-01-25
Jackson-Pratt Channel Drains Recalled for Multiple Performance Defects
Cardinal Health is recalling Jackson-Pratt Channel Drains due to performance defects including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. The recall affects 7,129 units distributed worldwide.
Product
Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2227
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0141-2023·2023-01-25
Ketorolac Tromethamine ophthalmic solution recalled due to manufacturing deviations
Akorn is recalling Ketorolac Tromethamine Ophthalmic Solution nationwide due to manufacturing practice deviations. The voluntary recall affects multiple lot numbers of the 0.5% formulation.
Product
Ketorolac Tromethamine Ophthalmic Solution, 0.5%, Packaged as a) 10 mL dropper bottle, NDC 17478-209-11; (b) 3 mL dropper bottle, NDC 17478-209-19; (c) 5 mL dropper bottle, NDC 17478-209-10; Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0972-2023·2023-01-25
Cardinal Health Jackson-Pratt Channel Drains recalled due to performance defects
Cardinal Health is recalling Jackson-Pratt Channel Drains (19 Fr, REF JP-2191) due to multiple performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken wound tips. Approximately 3,520 units were distributed worldwide.
Product
Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2191
Category
Medical Device
Distribution
Distributed nationwide