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.
4,310 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
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)
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)
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)
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)
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)
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)
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)
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)
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)
Reported Jun 22, 2016
Vaxcel PICC with PASV Catheter Kit under the following labels: 1) 3F, UPN H965454350, Rx ONLY, 2) 4F, UPN M001454550,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Navilyst Medical, Inc., an AngioDyamics Company
22 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 22, 2016
The XN-Series modules (XN-10, XN-20) are quantitative multi-parameter automated hematology analyzers intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex Corporation
FDA (openFDA device enforcement)
Reported Jun 22, 2016
Universal Battery Charger II (UBC II)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
CEFTRIAXONE for Injection USP, 250mg/vial, Rx only, MFG: LUPIN LIMITED INDIA, Packaged by Aidarex Pharmaceuticals, NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aidarex Pharmaceuticals LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jun 15, 2016
Honest Kids-Super Fruit Punch, Organic Juice Drink, 59 fluid oz. bottle, 006 57622 41273 7, Honest Tea, Inc., 4827…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coca-Cola Company (The)
FDA (openFDA food enforcement)
Reported Jun 15, 2016
GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Liko Universal SlingBars Universal SlingBar" 350, Universal SlingBar" 350 QRH, Universal SlingBar" 350 R2R, Universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Signature TKA GDE/MDL Set 04-05 Patient-specific surgical guide and instrument set.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materialise USA LLC
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Nuvi Global StemVitae Multivitamin 30oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nuvi Global Corporation
FDA (openFDA food enforcement)
Reported Jun 15, 2016
Sedecal SA Mobile Diagnost w DR x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal USA, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
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.