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 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

Reported Oct 13, 2021

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…

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

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…

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

Djo, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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

Flower Orthopedics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…

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

ZOLL Circulation, Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI…

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

Abbott Molecular, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 6, 2021

Dairy Free Co. Dollup Lama Sour & Creamy Cashew Topping 4oz, 6 containers per case

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

Central Kitchen Food Hub

FDA (openFDA food enforcement)

Food

Reported Oct 6, 2021

Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack

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

Keurig Dr Pepper

FDA (openFDA food enforcement)

Drugs

Reported Oct 6, 2021

Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total/Nighttime…

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

New Vision Pharmaceuticals LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 6, 2021

uMI 550 System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the…

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

Shanghai United Imaging Healthcare Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 6, 2021

Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case

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

Velvet Ice Cream Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 29, 2021

Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…

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)

Medical devices

Reported Sep 29, 2021

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…

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

In2bones USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only

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

Medtronic Perfusion Systems

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…

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

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190

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

Roche Molecular Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

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

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

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

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Food

Reported Sep 22, 2021

Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.

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

Jimmy's Cookies, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

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

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 13, 2021

SAS Foods Enterprises Inc. Recalls Frozen, Fully Cooked Beef and Chicken Empanada Products Packaged without Benefit of…

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

SAS Foods Enterprises Inc.

USDA FSIS

Food

Reported Sep 8, 2021

BrightFarms Sunny Crunch; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois…

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

Bright Farms

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical…

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

DePuy Orthopaedics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

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

Hostess Brands, LLC

1 more product in this recall

FDA (openFDA food 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.