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 Feb 17, 2016

Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are…

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

Zimmer Dental Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 12, 2016

McCain Foods USA, Inc. Recalls Pork Products Due To Possible Foreign Matter Contamination

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

McCain Foods USA, Inc.

USDA FSIS

Medical devices

Reported Feb 10, 2016

API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2016

Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and…

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

Draeger Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2016

Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by Mars Chocolate na, llc Hackettstown, NJ…

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

Mars Chocolate North America

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2016

Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…

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

Resmed Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2016

ADVIA Centaur PSA Assay; Catalog Number: 06574155/SMN 10310292 (100 test kit) and Catalog Number: 02676506/SMN 10310293…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2016

Biosure Driver, Product No: 72201887 For delivery and placement of orthopedic screws. Orthopedic Manual Surgical…

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

Smith & Nephew, Inc., Endoscopy Div.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2016

Zatarain's New Orleans Style RED BEANS AND RICE, ORIGINAL, NET WT 8 OZ, UPC 7142909849

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

Zatarain's Partnership, LP

FDA (openFDA food enforcement)

Medical devices

Reported Feb 3, 2016

Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…

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

Midmark Corp. dba Progeny Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2016

TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY. Indicated for use…

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

Abeon Medical Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2016

The e.cam Dual Signature Gamma Camera system. Used to detect or image the distribution of radionuclides in the body or…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in…

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

Bayer Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…

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

Skytron, Div. The KMW Group, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 20, 2016

TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED, 12-0.11OZ (3.2g)/ EA NET WT 1.34 oz (38g), UPC…

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

Twinings North America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 13, 2016

Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Smith & Nephew GENESIS(R) II/LEGION(TM) PATELLAR COMPONENT, RESURFACING ROUND, 32MM STANDARD, FOR CEMENTED USE ONLY…

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 Jan 13, 2016

The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman Pleural/Pneumopericardial Drainage Set consists of…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Food

Reported Jan 13, 2016

BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS: MILK, EGGS, WHEAT, SOY. MAY CONTAIN:…

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

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 6, 2016

Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 6, 2016

Friendly Farms Greek Peach Parfait Nonfat Yogurt net wt. 5.3 oz (150g) Distributed by ALDI Inc., Batavia, IL 60510

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

Ehrmann Arizona Dairy LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

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

Trumpf Medical Systems, Inc.

FDA (openFDA device 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.