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 1, 2026

Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

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

Waldemar Link GmbH & Co. KG (Mfg Site)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Battery Charging Station; Model: 0998-00-0802;

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

Datascope Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2026

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…

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

Winder Laboratories, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2026

HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Artelon FlexBand Dynamic Matrix Ref: 31057

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

International Life Sciences

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version:…

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

Medartis AG

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2026

VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***)…

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

Palmetto Gourmet Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2026

PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2026

Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…

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

Vascutek, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

PIE Trolley System Model: 2005

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

Edermy LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus…

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

Encore Medical, LP

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with…

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

MRIMed Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2026

NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA).…

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

Navitas, LLC.

FDA (openFDA food enforcement)

Food

Reported Mar 4, 2026

Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case

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

Sb Food LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…

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

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with…

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

Integra LifeSciences Corp. (NeuroSciences)

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 25, 2026

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid…

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

Pure Solutions, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…

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

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code: 00827002607842 REF:…

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 19, 2026

Sobico USA LLC Recalls Siluriformes Fish Products Imported Without The Benefit of Import Reinspection

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

Sobico USA LLC

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.