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 48,122 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Feb 15, 2017
Bakers Corner Vanilla Instant Pudding & Pie Filling, UPC 0 41498 15253 6 Distributed by ALDI; Best Choice Vanilla…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Subco Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Feb 15, 2017
DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Feb 15, 2017
InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Class I non-sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vertebral Technologies, Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported Feb 8, 2017
Hot Cocoa, NOT FOR RETAIL SALE, Prod: 28OCT2016, BB: 28JUN2017, Net Weight: 907 g (2.0 lb), Best Before: 28JUN2017
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arro Corporation
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 8, 2017
Mikesell's Nacho Cheese FLAVORED TORTILLA CHIPS 2.25 OZ (64g) bag UPC 0 71104 00554 3
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mike-Sells Potato Chip Co.
FDA (openFDA food enforcement)
Reported Feb 8, 2017
Olympus Scientific Solutions Americas Corporation (OSSA) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Scientific Solutions Americas
FDA (openFDA device enforcement)
Reported Feb 8, 2017
Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 1, 2017
Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50Kg sizes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumedia Manufacturers, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Hitachi Oasis MRI System - C-Spine Coil
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007. Delivers INOMAX (nitric oxide for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INO Therapeutics (dba Ikaria)
FDA (openFDA device enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
FPI Breaded Round Shrimp Tail-On 1001990, 12-8 oz. cartons per master case, Master case 6 lbs. (2.72 kg)
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Liner Foods, Inc.
FDA (openFDA food enforcement)
Reported Jan 25, 2017
PREMIER EHEC and PREMIER EHEC Bulk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jan 18, 2017
In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brand Castle LLC
FDA (openFDA food enforcement)
Reported Jan 18, 2017
SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Medline E-Z Lubricating Jelly; Bacteriostatic. Water Soluble. Sterile. 2 FL OZ (59 ml). Product Usage: For medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Ind
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Manufacturing Limited
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Indiana recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.