Recalls distributed in Ohio
These notices name Ohio 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.
5,400 stored notices name Ohio, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Ohio too — those are in the archive.
Reported Apr 15, 2015
Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bacterin International, Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2015
CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2015
Gourmet Foods Mamma-Italia Traditional Italian Raw Pizza Dough Ball, Box Quantity: 30 16 oz BALL Keep Frozen NET WT: 30…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dough Acquisition Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 15, 2015
Giant Eagle Irish Soda Bread, 16oz loaf, in plastic wrap, one 16oz loaf per wrapped package
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 15, 2015
Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Boston Scientific: Expel" Drainage Catheter with Twist-Loc" Hub APDL Drainage Catheter and APDL Drainage Catheter Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gilster-Mary Lee Corp.
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
MR. HYDE INTENSE ENERGY PRE WORKOUT, Green Apple Natural and Artificial Flavor Dietary Supplement Net Weight 8.0 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSupps USA LLC
FDA (openFDA food enforcement)
Reported Apr 8, 2015
LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
The package reads in part "***Northern Chef***GLUTEN FREE, OVEN READY LIGHTLY COATED COD***KEEP FROZEN/DO NOT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tai Foong U.S.A., Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Diamondback 360 Coronary Orbital Atherectomy System, Model Number: DBEC-125. The system is indicated to facilitate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardiovascular Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.fgf brands, Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2015
GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Stonewall Kitchen Buffalo Wing Sauce Net Wt. 17.5 oz. glass jar UPC 711381-31395 4 Item # 251805,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2015
Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Titan Spine, LLC
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Wal-Mart private label " the Bakery baked with pride," Sock It To Me Cr¿me Cake, Net Wt. 32oz (2lb) 907g, (packed in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Benson's Old Home Kitchens Bakery Division
FDA (openFDA food enforcement)
Reported Mar 25, 2015
Crea A and B membranes, packaged 4 per box Used in conjunction with the ABL800 FLEX analyzers which are intended for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America 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.