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 Jul 20, 2016

HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…

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

Heartware, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…

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

Synthes (USA) Products LLC

17 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2016

Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT 3.5 OZ (99G) INGREDIENTS: SUNFLOWER KERNELS, COTTONSEED…

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 13, 2016

The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…

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

Custom Ultrasonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2016

GE Healthcare, Discovery MR750w

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2016

Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy

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

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

Bigger-Better-Bladder With 3/8" ID tubing, ITEM BBB38

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

Circulatory Technology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

IMPAK Liquid Acrylic Resin sold under the following labels: 1) IMPAK PF PINK-FIBERED ELASTIC ACRYLIC RESIN LIQUID, 11…

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

CMP Industries, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

MOSAIQ Oncology Information System

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

Saw Sagittal Catalog Number: ES 300; Saw Sagittal Refurbished Catalog Number: ES300-R; Saw Saggital, Finger Catalog…

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

Medtronic Sofamor Danek USA, Inc. - Dallas Distribution

FDA (openFDA device enforcement)

Food

Reported Jul 6, 2016

Productos Del Campo Castillo Chile Habanero (Fresh Habanero Peppers)

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

Montero Farms

FDA (openFDA food enforcement)

Food

Reported Jul 6, 2016

Reser's Deviled Egg Potato Salad, Refrigerated, Retail package, Net wt. 3 lbs. UPC 0 71117 00480 9; Reser's Deviled Egg…

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

Reser's Fine Foods, Inc. - Century

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 6, 2016

Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module…

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

Siemens Healthcare Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

Syngo.plaza, Picture archiving and communication system (PACS), Model Numbers - 10863171, 10863172, 10863173,

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 6, 2016

simple truth organic Mixed Vegetables NET WT 10 OZ (283g) KEEP FROZEN INGREDIENTS: ORGANIC CARROTS, ORGANIC CORN…

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 29, 2016

Golden Gourmet Snacks Veggie Chips; Net Wt. 12 OZ; Bickel's Snack Foods, Inc., York, PA 17404 Lot codes: 26SEP16 Z4D1…

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

Bickel's Snack Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Jun 29, 2016

Dakota Style Roasted & Salted Sunflower Kernels, Net Wt. 3.5 oz. plastic bag. UPC 84872-20172

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

Dakota Style, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 29, 2016

Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal antigens and positive controls are used to…

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

Immuno-Mycologics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 29, 2016

Myriad handpiece Tissue morcellator

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

Nico Corp.

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2016

Big Sur Breakfast Burrito; A delicious blend of roasted potatoes & red peppers, smoked seitan and seasoned tofu. Net…

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

Sweet Earth Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 22, 2016

BioSync Anatomic Cotton Wedge, 16 x 4.5 mm.; Used for internal bone fixation for bone fractures, fusions or osteotomies…

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

Arthrex, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 22, 2016

Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Guide Wire for fixation of fractures that occur in and…

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

CarboFix Orthopedics, Ltd.

FDA (openFDA device 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.