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 Apr 12, 2023

Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Description: 17533-04 DR GROSS LPS LLC 18704-03 CATARACT…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305

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

Fujifilm Irvine Scientific, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2023

BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2023

DeRoyal SafeLiner Suction Canister, 1000cc, REF PHESL-1000B

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 29, 2023

DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).

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

Dollar General Corporation

FDA (openFDA food enforcement)

Food

Reported Mar 29, 2023

Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag, containing individually wrapped pieces. UPC…

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

Russell Stover Candies Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 29, 2023

Haiyue Food Nutritional Preserved Vegetable

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

Xiumin Lin

FDA (openFDA food enforcement)

Meat & poultry

Reported Mar 24, 2023

Elkhorn Valley Packing Recalls Boneless Beef Chuck Product Due to Possible E. coli O103 Contamination

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

Elkhorn Valley Packing LLC

USDA FSIS

Medical devices

Reported Mar 22, 2023

Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 22, 2023

Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.

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

Brainlab AG

FDA (openFDA device enforcement)

Food

Reported Mar 22, 2023

Fruit flavored ready-to-eat cereal packaged in 1.27 oz. (UPC 850017468214) and 8oz. ( UPC 850017468085) plastic stand…

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

Catalina Snacks

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 22, 2023

Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box

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

Keurig Dr Pepper

FDA (openFDA food enforcement)

Medical devices

Reported Mar 22, 2023

Fusion Bioline Vascular Graft, Part number M00201503046B0

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

Maquet Cardiovascular, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 22, 2023

ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US

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

Mead Johnson & Company

FDA (openFDA food enforcement)

Medical devices

Reported Mar 22, 2023

Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090

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

Scientia Vascular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

LATITUDE NXT Remote Patient Management System, LATITUDE NXT System Server Software Model 6460.

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2

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

DiaSorin Molecular LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 15, 2023

Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…

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

Given Imaging Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…

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

Preat Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

Sensus Healthcare Inc, SRT-100 Vision IPX 0, HFUS Module IPX 1, with software version 1.9.2; Superficial X-ray…

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

Sensus Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 8, 2023

HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…

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

Alpenland International, Inc.

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.