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.

4,253 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.

Medical devices

Reported Apr 17, 2019

SORIN Heater-Cooler System 3T, REF 16-02-85 Intended for use with a Stockert/Sorin S3/S5/C5 heart-lung machine and/or…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301…

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

Procept Biorobotics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 10, 2019

The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 10, 2019

Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame…

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

Century Snacks LLC

FDA (openFDA food enforcement)

Drugs

Reported Apr 10, 2019

Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: The Kroger Co, Cincinnati, OH…

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

Legacy Pharmaceutical Packaging LLC

FDA (openFDA drug enforcement)

Food

Reported Apr 3, 2019

Modjeskas Bauer's Candies NET WT 8 oz, 12 oz, 16 oz, 32 oz. boxes & 4 oz, 8 oz bags, 400 pc case, 216 pc case

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

Bauer's Candies, Inc.

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 3, 2019

Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous Autotransfusion System) is indicated for the…

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

Fenwal Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 3, 2019

Quinoa, 16 oz plastic package

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

The Kroger Company

FDA (openFDA food enforcement)

Food

Reported Mar 27, 2019

Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6…

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

Horizon Food Group

2 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Mar 27, 2019

Losartan Potassium Tablets, USP, 25 mg, 30 tablet bottles, Rx Only, Distributed by: Wal-Mart, Bentonville, AR 72716,…

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

Legacy Pharmaceutical Packaging LLC

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Mar 27, 2019

Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottle (NDC: 68788-0048-03), b) 90-count bottle (NDC:…

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

Preferred Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 27, 2019

smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1 SIZE, STEM, REF 713552510

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

Smith & Nephew, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2019

Cook Transseptal Needle, Reference Number TSNC-18-71.0, Order Number G02364. For transseptal left heart access in both…

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

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2019

Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in…

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

Ossur Americas

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2019

Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate…

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

Perrigo Company PLC

FDA (openFDA food enforcement)

Food

Reported Mar 13, 2019

DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…

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

Kingston Pharma LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2019

Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2019

Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.

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

Rvo 2.0, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2019

Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…

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

Alcon Research Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Phoenix AST-s Indicator, Catalog Number 246009

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

Becton Dickinson & Co.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure…

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

Cook Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2019

Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…

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

King Orchards

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.