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.

4,310 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

Reported Jul 12, 2017

Jelco, Hypodermic needle Pro¿ needles 19G X1 1/2" 800/CA Model No. EL 1915 & 19G X 2" 600/CA Model No. SB 5021, Rx…

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2017

Exactech 1.5" Novation Calcar Planer Guide Tip To assist the surgeon in the implantation of Novation hip system…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 5, 2017

SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number: CH-200/CH-200M Holds an x-ray tube unit and…

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

Shimadzu Medical Systems USA Com

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 5, 2017

Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz (184g) INGREDIENTS: ***NONFAT M ILK***CONTAINS: WHEAT, EGGS, SOY.…

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

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Jun 28, 2017

GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222.

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

Genetic Edge Compounds LLC

FDA (openFDA food enforcement)

Food

Reported Jun 28, 2017

Meijer Honey Vanilla Bourbon Pecans, 8.5 oz., 6/case, packed in a stand-up pouch.

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

Meijer, Inc. #816 - Grand River Packaging

FDA (openFDA food enforcement)

Food

Reported Jun 28, 2017

PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…

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

Monfitello

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 28, 2017

Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates…

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

Omega Medical Imaging, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 28, 2017

Southern Grove Cashew Halves & Pieces with Sea Salt, Net Weight 8.0 oz. (227 grams)

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

Star Snacks Co., Llc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 28, 2017

Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 28, 2017Updated Oct 23, 2026

Vinh Hoan USA, Inc. Recalls Siluriformes Fish Products Due To Failure To Comply With FSIS Import Requirements

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

Vinh Hoan USA, Inc.

USDA FSIS

Food

Reported Jun 21, 2017

Chocolate chip cookie dough larabars, 10 count , UPC 100-21908-49031 incorrectly packaged in peanut butter cookie…

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

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 21, 2017

Philips DigitalDiagnost 3.1.x X-Ray System

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

Philips Electronics North America Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 21, 2017

Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel…

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

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Jun 21, 2017

Simple truth Dry Roasted Macadamia Nuts SEA SALT 12 oz bag UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI,…

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

The Kroger Co.

FDA (openFDA food enforcement)

Meat & poultry

Reported Jun 20, 2017

Channel Fish Processing Co., Inc. Recalls Siluriformes Fish Products Due To Misbranding and Undeclared Allergens

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

Channel Fish Processing Co., Inc.

USDA FSIS

Food

Reported Jun 14, 2017

California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola…

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

California Sun Dry Foods

FDA (openFDA food enforcement)

Medical devices

Reported Jun 14, 2017

DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 14, 2017

Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…

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

Acumed LLC

FDA (openFDA device enforcement)

Food

Reported Jun 7, 2017

Kite Hill Mushroom and Ricotta Ravioli; frozen Ravioli made with almond milk ricotta: 9 oz. package. UPC 856624004173…

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

Lyrical Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 7, 2017

NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F

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

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 5, 2017Updated Oct 23, 2026

Creation Gardens Inc. Recalls Ground Beef and Beef Primal Cut Products Due to Possible E. coli O157:H7 Contamination

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

Creation Gardens

USDA FSIS

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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.