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.
4,312 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Mar 13, 2013
Philips Medical System Extended Brilliance Workspace (EBW), Computed Tomography X-Ray System. The Extended Brilliance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
ALL NATURAL ANCIENT GRAIN BREAD, NET WT. 13.8 OZ. (393 g), PRODUCT OF CANADA, UPC 0 49800 08712 5 (appears on bag),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 13, 2013
AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Stryker XIA 3 Iliac Screwdriver, 3-PCS. The XIA 3 Iliac Screwdriver is used to drive XIA 3 closed head Monoaxial and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Animas Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2013
LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
MAYFIELD¿ Composite Series Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
FDA (openFDA food enforcement)
Reported Feb 27, 2013
Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2013
The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lumenis Limited
FDA (openFDA device enforcement)
Reported Feb 20, 2013
Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Feb 20, 2013
Pamela's Baking and Pancake Mix; Gluten Free, Wheat Free 24 oz package. UPC 93709-30010 Pamela's Products, Ukiah, CA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pamela's Products, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2013
The product is a lyophilized growth supplement for use with dehydrated culture media to prepare BCYE Medium used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2013
St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Jude Medical Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
KODAK INSIGHT DENTAL FILM in SureSoft Packets, Size 2 Single Packet Film, Model Number IP21S, REF/Catalog Number…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Carestream Health, Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diagnostic Hybrids Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2013
BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Chocolate Covered Coconut Balls is packaged in either 2-ounce packages (2 pieces per package) or in 0.5 lb and 1 lb.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chocolate Decadence
FDA (openFDA food enforcement)
Reported Feb 6, 2013
Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
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.