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.
4,309 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Jul 31, 2019
ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2019
BBQ Bread & Pull-A-Part BBQ Bread sold under the brand names of Flowers UPC 7 22500 40792, Ingles UPC 8 68540 15348 &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods
11 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2019
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FoodScience Corporation
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Conagra Brands, Inc. Recalls Canned Beef Products Due to Possible Processing Defect
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hometown Food Company
USDA FSIS
Reported Jul 31, 2019
Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jelly Belly
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medela Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Ragu Chunky Sauce Tomato, Garlic & Onion 45oz and 66oz retail sizes sold in plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizkan America, Inc. - Corporate
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Terumo Sur-vet Needle, 20G x 1", Product Code 100204
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Medical Corporation
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-LP polyaxial screws -…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clariance Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
White Cheddar 5906-KD is a non-GMO White Cheddar Cheese Blend dried cheese powder. Product was shipped in bulk bags,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Commercial Creamery Company
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Advincula Delineator with Ultem Plastic Soft Cup size 2.5 cm; Part No. AD750SC-KE25 The Advincula Delineator Uterine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
The Tina-quant lgA Gen.2 is an immunoturbidimetric assay. Anti-lgA antibodies react with antigen in the sample to form…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Raw fresh whole jalapeno, ambient Non-descript 10# cardboard box. Sold as 10lb unit or by the pound.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shelton Farms dba Shelton's Wholesale Co.
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wilton Brands
FDA (openFDA food enforcement)
Reported Jul 17, 2019
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Jul 17, 2019
ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The Revive bladder support is intended for temporary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rinovum Women's Health
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging sources, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent, Product Number HY0305Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food 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.