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 Jul 24, 2013
Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus Product Usage: Angiographic x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2013
nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2013
Talenti Gelato, Toasted Almond, One Pint (473ml), Crafted by: Talenti, Marietta, GA 30062
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talenti Gelato
FDA (openFDA food enforcement)
Reported Jul 24, 2013
CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
ARO Pistachios, Pistachios raw kernel - no salt; Sold in 9 oz. raw kernel, no salt airtight jar; 2.5 lb raw Kernel, no…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARO Pistachios, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 17, 2013
REF 154200 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size A3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
29 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Jul 17, 2013
***REF C7120***APEX Arthroscopy Tubing Set. Intended for use for joint irrigation and dissention during arthroscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linvatec Corp. dba ConMed Linvatec
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
Item Number: 101643 Item Description: TUB CHOC DD PEANUTS Case Pack: 12 Package Size: 8 OZ 2-Piece Clear Tub (Zoppity…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
51 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 10, 2013
Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cheryls
FDA (openFDA food enforcement)
Reported Jul 10, 2013
HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clorox Healthcare Holdings, LLC (dba HealthLink)
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
1) VITROS 5,1 FS Chemistry System (product code 6801375) and 2) VITROS 5,1 FS Chemistry System Refurbished (product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile 4305-19-40. Used in retracting the humeral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Enzyme Solutions, A Dietary Supplement, Formula 29, 8 oz. (226.8g), UPC Code 697706041408. Distributed by: Enzyme…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Enzyme Formulations, Inc.
FDA (openFDA food enforcement)
Reported Jul 3, 2013
GE Healthcare Senographe Essential System. The Senographe 2000D system generates digital mamnmographic images that can…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2013
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrad Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation Systems. Product Usage: The Phoenix Retrograde…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Jun 26, 2013
Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
Market Pantry, Sweet & Salty Mix, NET WT 3 oz (85g), UPC 0 85239 08131 0, INGREDIENTS: Peanuts (peanuts...) ...Honey…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Importing Co., Inc.
FDA (openFDA food 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.