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 Jan 29, 2014
XiO RTP System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2014
VITROS Chemistry Products COCM Reagent
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 29, 2014
ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Draeger Infinity Acute Care System Monitoring Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Healthcare It
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Hot Smoked Wine Maple Salmon, Item HS-B, vacuum packaged and either frozen or refrigerated, ranging in size between…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Josephson's Smokehouse
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 22, 2014
Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Newcastle Ltd.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2014
Illinois Firm Recalls Sliced Spiral Hams for Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Carl Buddig and Company
USDA FSIS
Reported Jan 15, 2014
Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Sandel Medical Industries LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Medical Corporation
FDA (openFDA device enforcement)
Reported Jan 15, 2014
SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 15, 2014
NanoClave Connector, Part No. A1000, Item No. 011-A1000, 061-A1000, A1000, K7083-001, Z3769 The ICU Needleless…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
49 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2014
AdvanDx Gram-Negative QuickFISH BC. In-Vitro Diagnostic for the identification of Enterobacteriacae Catalog Number:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.AdvanDx, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2014
VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2014
Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quaker Foods and Snacks North America
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2014
Macaroni Reg CAD, Formula MA.50, Macaroni Salad, packaged: -7-Eleven Fresh to Go Macaroni Salad, 12/7-oz carton cases.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
212 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2014
Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
outer box: Ref 906768, CurvTek Eye Needle 22 MM X-large Stainless Steel, Single Use Gamma Sterilized, Rx inner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Flora Double Ginger Herbal Tea Blend, 16/1.24 oz (35.2g) tea bags per package. UPC 0 61998 63757 9 The product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flora Inc.
FDA (openFDA food enforcement)
Reported Dec 25, 2013
Garden-Fresh,,1/4" x 1" Green Pepper Sticks, 2/2 lb., 0 11596 40586 5 11/9/2013-11/11/2013; Garden-Fresh, Green Pepper…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Garden-Fresh Foods, Inc.
254 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 25, 2013
Bremer Garlic Shrimp MEAL IN MINUTES Pasta in Garlic Sauce with Broccoli, Shrimp, Corn and Carrots 21 oz bags,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gourmet Express LLC
FDA (openFDA food enforcement)
Reported Dec 25, 2013
VITROS CA 125 II Calibrators For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, VITROS 3600…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
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.