Recalls distributed in Indiana
These notices name Indiana in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Jan 1, 2025
EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical
FDA (openFDA device enforcement)
Reported Jan 1, 2025
BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straight Smile, LLC
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Bulk salt product shipped in 1 metric ton tote; 50lb bag Special Purity Granulated Food-Grade Salt with UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Minerals America Inc.
FDA (openFDA food enforcement)
Reported Dec 25, 2024
Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fabalish,
FDA (openFDA food enforcement)
Reported Dec 25, 2024
OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Cucumbers Slices 1/2 Cup, 100 cups per case, Product Code CUCS100, Item Number - 14705 Cucumbers Diced 1" Peeled 5 lb.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Indianapolis Fruit Company, Inc.
FDA (openFDA food enforcement)
Reported Dec 25, 2024
Galaxy System (GAL-001)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical
FDA (openFDA device enforcement)
Reported Dec 18, 2024
BD Pyxis MedStation ES, REF: 323
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2024
Mama Mancini s Stuffed Shells with Sauce and Mozzarella Cheese, 4 packs of 4 lbs. each / 6 packs of 14 oz. each, 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Joseph Epstein Food Enterprises, Inc. dba MamaMancini's
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 18, 2024
Nestle Health Services Nutren 2.0 kCal/mL, Calorically Dense Complete Nutrition with Fiber Unflavored. 1000mL (1.1QT).…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Health Science
FDA (openFDA food enforcement)
Reported Dec 18, 2024
Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical
FDA (openFDA device enforcement)
Reported Dec 18, 2024
CIBUS Fresh, Jack & Olive, Sprig and Sprout branded Autumn Turkey Sandwich 9.65oz UPC 00810028251915
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Piazza Produce (dba CIBUS Fresh)
FDA (openFDA food enforcement)
Reported Dec 18, 2024
Fresh Gourmet TORTILLA STRIPS SANTA FE SYTLE NET WT 3.5 OZ (99g) UPC 7 87359 17504 6 DISTRIBUTED BY: FRESH GOURMET CO.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sugar Foods LLC
FDA (openFDA food enforcement)
Reported Dec 18, 2024
Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tipp Distributors, Inc. dba Novamex
FDA (openFDA food enforcement)
Reported Dec 11, 2024
(1) READY MEALS GREEN CHILI CHICKEN ENCHILADAS SS COLD (UPC 21291600000) (2) GREEN CHICKEN ENCHILADAS 6 CT SS COLD (UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Albertsons Companies LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cartiva, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2024
Member's Mark brand Roasted Red Pepper Hummus; 32 oz (907 g) Plastic Container with UPC# 193968044268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cedar's Mediterranean Foods, Inc.
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Organic Hot Agave in the Raw, 10 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cumberland Packing Corp.
FDA (openFDA food enforcement)
Reported Dec 11, 2024
Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279407074 and Case…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2024
EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 11, 2024
Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 11, 2024
BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.