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 Apr 23, 2025

Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro…

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

Maquet Cardiovascular, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel; REF: 037.3002;

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

Straumann USA LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

t:slim X2 Insulin Pump with Interoperable Technology

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

Tandem Diabetes Care, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with…

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

Thoratec LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2025

Dr. Praeger s California Veggie Fries 8oz,

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

Dr. Praeger's Sensible Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2025

Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072…

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

Qapel Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 9, 2025

Tostitos Cantina Traditional Yellow Corn Tortilla Chips. Net Wt. 13oz. (368.5) UPC 0 28400-52848 1. Frito-Lay, Inc.,…

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

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Food

Reported Apr 9, 2025

Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…

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

Nestle-USA, Inc. (Corporate Office)

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2025

Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version:…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 5, 2025

Johnsonville, LLC, Recalls Cheddar Bratwurst Product Due to Possible Foreign Matter Contamination

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

Momence Real Estate

USDA FSIS

Medical devices

Reported Apr 2, 2025

CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of…

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

Calyxo, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 2, 2025

COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ…

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

Massimo Zanetti Beverage USA

FDA (openFDA food enforcement)

Medical devices

Reported Apr 2, 2025

CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web…

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

St. Jude Medical

FDA (openFDA device enforcement)

Food

Reported Apr 2, 2025

DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING…

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

U.S. Tov, Inc. dba U.S. Trading Company

FDA (openFDA food enforcement)

Medical devices

Reported Mar 26, 2025

Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.

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

B Braun Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.

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

FUJIFILM Healthcare Americas Corporation

FDA (openFDA device enforcement)

Food

Reported Mar 26, 2025

Berry Buddies; Blueberries, Mini Pancakes & Real Maple Syrup; NET WT 2.1 oz (60 g); 3-compartment non-flex plastic…

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

Naturipe Value Added Fresh LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…

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

Oridion Medical 1987 Ltd.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for…

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

Remel, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 26, 2025

HOT ONES brand VERDE, Los Calientes Hot Sauce, BY HEATONIST; 1 gallon, 5 oz, and 5 gallon sizes; UPC: 8-51444-00803-5

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

The Karma Sauce Company LLC

1 more product in this recall

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.