All recall categories

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.

Medical devices

Reported Aug 31, 2022

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 24, 2022

(1) CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads 5 in. x 9 in. per box, ASO Item No. 781083, SKU…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aso LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 24, 2022

FSIS Issues Public Health Alert for Poultry and Meat Products Containing FDA-Regulated Corn Starch That Has Been…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Food

Reported Aug 24, 2022

Fancy Buckwheat Flour, Item #327, 50 lbs. net wt, Packed by Min-Dak Growers Grand Forks, ND - Product of the USA.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Minn Dak Growers, Ltd.

FDA (openFDA food enforcement)

Food

Reported Aug 24, 2022

Sweet Loren's Place and Bake Sugar Cookie Dough, Net Wt. 12 oz.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sweet Loren's

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aesculap Implant Systems LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2022

The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 17, 2022

Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Refresco Beverages US Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

cobas e801 Immunoassay Analyzer

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2022

Xhibit Telemetry Receiver, Model: 96280

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aesculap Implant Systems LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g

High riskUsing this product could cause serious injury, illness or death — stop using it now.

MKS Enterprise LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 10, 2022

UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Neotract Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

St. Jude Medical, Cardiac Rhythm Management Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Procter & Gamble Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 3, 2022

Bumble Bee Smoked Clams Shucked Easy Open NET WT. 3.75 oz. (106 g) Distributed By: Bumble Bee Seafoods San Diego, CA…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bumble Bee Foods, LLC

FDA (openFDA food enforcement)

Food

Reported Aug 3, 2022

Simply Nature Organic Spring Mix 16 oz. Marketside Spring Mix 11 oz. and 5 oz.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2022

Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

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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.