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.
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)
Reported Jun 8, 2016
Hip Preservation System Signature Series PreBent Burs under the following labels: 1) PreBent Spherical Bur, 5.5mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Walnut Delights 6 Pack Net Weight: 9 oz. PLU #69690 UPC: 2 69690 20399 7 Giant Eagle, LLC, Pittsburgh, PA
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Torque Limiting Handle: PRECIMED, T-Handle Torque, Non Sterile. Handle: Customer Number/Model: MCL120014 T14000,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greatbatch Medical
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Novocastr Liquid Mouse Monoclonal Antibody Renal Cell Carcinoma Marker (RCC) is recommended for use as part of a panel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Liquid Assets Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics 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.