State

Indiana product recalls

73,376 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: 2,528
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 2,528 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20301–20325 of 82963

HighFDA (Food)·F-0051-2023·2022-10-26
Tuscan Garden Italian Dressing Recalled for Undeclared Soy and Wheat Allergens
Tuscan Garden Restaurant Style Italian Dressing is being recalled due to undeclared soy and wheat allergens. The recall affects 26,370 mixed cases distributed across 20 states.
Product
Tuscan Garden Restaurant Style Italian Dressing , Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case containing 3 Dressing flavors, including 8 bottles of the Restaurant Style Italian
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0095-2023·2022-10-26
BD Vacutainer Blood Alcohol Testing Tubes Recalled for Analytical Interference
BD Vacutainer blood collection tubes are recalled due to isobutylene contamination that may cause false positive results in blood alcohol testing.
Product
BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0093-2023·2022-10-26
Siemens N Antiserum to Human IgG Recall for High-Dose Performance Failure
Siemens Healthcare Diagnostics recalls N Antiserum to Human IgG reagent for laboratory analyzers because it does not meet expected High-Dose Hook Effect performance specifications for IgG measurements in certain sample types.
Product
N Antiserum to Human IgG, 2mL Variant for BN II System and BN ProSpec System-IVD Siemens Material Number (SMN): 10446297
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0015-2023·2022-10-26
Saline Solution Injection Recalled Nationwide Due to Sterility and Leakage
Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection distributed nationwide due to lack of assurance of sterility and potential leakage. Multiple lot numbers with expiration dates ranging from May 2023 to August 2023 are affected.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0091-2023·2022-10-26
IV Extension Sets Recalled for Bonded Joint Failure and Leakage Risk
B. Braun extension sets (Product Code 470169) are recalled due to high probability of bonded joint failure, which may cause leakage or detachment during use, risking bloodstream infections and medication exposure.
Product
Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per carton. A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood upon insertion of a male luer connector.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0053-2023·2022-10-26
Lyons Ready Care Thickened Orange Nectar Recalled for Spoilage
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Nectar due to indication of product spoilage. The recall affects 1,272 cases distributed nationwide with specific lot numbers and best-by dates in March 2023.
Product
Lyons Ready Care Thickened Orange Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Food)·F-0064-2023·2022-10-26
Nestle Cookie Dough Recalled for Plastic Contamination
Nestle-USA is recalling Stuffed Chocolate Chip Cookie Dough due to consumer complaints of white plastic pieces found in the product. Consumers should not eat the product.
Product
"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"
Category
Food
Distribution
40 states
HighFDA (Food)·F-0057-2023·2022-10-26
Lyons Ready Care Thickened Sweet Tea Recalled for Product Spoilage
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Sweet Tea with Lemon Nectar due to indication of product spoilage. Approximately 491 cases were distributed across all U.S. states.
Product
Lyons Ready Care Thickened Sweet Tea with Lemon Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Food)·F-0069-2023·2022-10-26
Tastykake Glazed Cherry Pie Recalled Due to Undeclared Soy Lecithin
Flowers Foods is recalling Tastykake Glazed Cherry Pie due to undeclared soy lecithin in the product. The recalled product may pose a health risk to consumers with soy allergies.
Product
TASTYKAKE GLAZED CHERRY PIE NET WT 4.5 OZ (128g) UPC 0 25600 00969 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0098-2023·2022-10-26
Synthes Orthopedic Implant Drill Kit Recall: Incorrect Drill Guide Size
Synthes (USA) Products LLC is recalling 81 SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kits nationwide due to incorrect drill guide sizing. The defect could result in bone damage and incorrectly placed drill holes during orthopedic surgery.
Product
SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No. SE-2020-10. Used with DePuy Synthes SPEEDSHIFT Continuous Compression Staple Implants for bone fixation and management of fracture and reconstructive surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V805000·2022-10-26
Sunset Park & RV Recalls 2022 Sun Lite and Rush Travel Trailers
Sunset Park & RV is recalling 2022 Sun Lite and Rush travel trailers because a welded seam on the awning fabric may separate, causing the awning to drop unexpectedly.
Product
SUNSET PARK & RV — SUNSET PARK & RV SUNLITE, RUSH
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0065-2023·2022-10-26
Mrs. Freshley's Apple Fruit Pie recalled for undeclared soy allergen
Flowers Foods is recalling Mrs. Freshley's Apple Fruit Pie (4.5 oz) because some packages may contain undeclared soy lecithin, a major allergen. Consumers with soy allergies should not consume the affected product.
Product
Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0089-2023·2022-10-26
Dimension Vista HDLC Reagent Cartridge Recalled for Inaccurate Lab Results
Siemens is recalling 1,592 units of Dimension Vista HDLC reagent cartridges due to potential for erroneous test results. Affected cartridges may produce falsely high or low HDL cholesterol measurements.
Product
Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent cartridge, IVD Siemens Material Number (SMN): 10464340 Catalog Number: K3048A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0067-2023·2022-10-26
Tastykake Glazed Apple Pie Recalled for Undeclared Soy Allergen
Flowers Foods is recalling Tastykake Glazed Apple Pie because soy lecithin is not declared on the labels. People with soy allergies could be at risk.
Product
TASTYKAKE GLAZED APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 00972 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0107-2023·2022-10-26
Medicina ENFit enteral syringe recall due to material specification defect
Medicina is recalling ENFit 1ml enteral syringes because the plunger was manufactured with polyethylene instead of approved polypropylene. This material defect could affect plunger function and device safety.
Product
Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0114-2023·2022-10-26
Medicina Reusable Oral Syringe recalled for incorrect plunger material
Medicina Uk Ltd is recalling Medicina Reusable Oral Syringe 2.5ml units because plunger components were manufactured with polyethylene instead of the specified polypropylene material.
Product
Medicina Reusable Oral syringe 2.5ml Code: OTH25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0111-2023·2022-10-26
Medicina Oral Tip Syringe recalled for unapproved plunger material
Medicina Uk Ltd is recalling Medicina Oral Tip Syringe 2.5ml nationwide because the plunger component was manufactured with polyethylene instead of the approved polypropylene material.
Product
Medicina Oral Tip Syringe 2.5ml Code: OT25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0070-2023·2022-10-26
Tastykake Glazed Lemon Pie Recalled for Undeclared Soy
Flowers Foods recalled Tastykake Glazed Lemon Pies due to undeclared soy lecithin in certain packages. Products with Enjoy By dates of Oct. 28, 31, Nov. 4, and 7 are affected.
Product
TASTYKAKE GLAZED LEMON FLAVORED PIE NET WT 4.5 OZ (128g) UPC 0 25600 00967 3 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0117-2023·2022-10-26
MitraClip G4 and TriClip G4 Cardiac Devices Recalled for Clip Locking Malfunction
Abbott has recalled MitraClip G4 and TriClip G4 cardiac repair devices due to clip locking malfunctions that may prevent proper device deployment. These malfunctions could lead to failed procedures and serious complications including device embolization.
Product
Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT, MitraClip G4 CDS NTW REPAIR-MR Clinical/CDS0704-NTW, MitraClip G4 CDS XT REPAIR-MR Clinical/CDS0704-XT, MitraClip G4 CDS XTW REPAIR-MR Clinical/CDS0704-XTW, TriClip NT Clip Delivery Sys CLIN/TCDS0203-NT…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0056-2023·2022-10-26
Lyons Ready Care Thickened Cranberry Honey Nectar Recalled for Product Spoilage
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Cranberry Honey Nectar due to indication of product spoilage. The recall involves 468 cases distributed across 49 states.
Product
Lyons Ready Care Thickened Cranberry Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
ModerateFDA (Food)·F-0059-2023·2022-10-26
Imperial Thickened Orange Nectar Recalled for Product Spoilage
Lyons Magnus LLC is recalling Imperial Thickened Orange Nectar due to indication of product spoilage. The 46 fl oz cartons were distributed nationwide.
Product
Imperial Thickened Orange Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
ModerateFDA (Food)·F-0052-2023·2022-10-26
Lyons Ready Care Thickened Apple Nectar Recalled for Product Spoilage
Lyons Magnus LLC recalls Lyons Ready Care Thickened Apple Nectar in 46 fl oz cartons due to product spoilage. Affected products were distributed nationwide.
Product
Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
ModerateFDA (Devices)·Z-0103-2023·2022-10-26
Optima Coil System Pouch Labels Do Not Match Carton Labels
BALT USA is recalling Optima Coil System models OPTI0208CSS10 and OPTI0308CSS10 due to a labeling discrepancy where pouch labels do not match carton labels. These endovascular devices require verification before use.
Product
Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0014-2023·2022-10-26
OTC Sinus Pressure and Pain Cough Product Mislabeled as Decongestant-Free
Walgreens Sinus Pressure, Pain & Cough tablets are mislabeled as 'Decongestant Free' but contain Phenylephrine HCl, a nasal decongestant. The labeling error affects 66,384 boxes distributed nationwide.
Product
SINUS PRESSURE, PAIN AND COUGH — SINUS PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0108-2023·2022-10-26
Medicina ENFit Enteral Syringes Recalled for Incorrect Plunger Material
Medicina Uk Ltd is recalling Medicina ENFit 5ml Reusable Enteral Syringes because the plunger component was manufactured with polyethylene instead of the specified polypropylene material.
Product
Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05
Category
Medical Device
Distribution
Distributed nationwide