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 Jul 11, 2018
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Absonutrix
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Amalgatome SD, COAXIAL PNEUMATIC HOSE, SCHRADER, Model X101004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exsurco Medical
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Star Wholesale Inc.
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Single Chamber Temporary External Pacemaker, Model 53401
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 4, 2018
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Safe N Simple No-Sting Skin Barrier Film, Ostomy Skin Barrier Wipe, SNS00807
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safe N Simple, LLC
FDA (openFDA device enforcement)
Reported Jul 4, 2018
ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
CritiCore Automated Urine Output and Temperature Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Cryovalve(R) SG Pulmonary Human Heart Valve, Catalog Number SGPVVOO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CryoLife, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The CARESCAPE R860 ventilator is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datex-Ohmeda, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kellogg Company
FDA (openFDA food enforcement)
Reported Jun 27, 2018
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Birmingham Hip Resurfacing Femoral Head: (a) Size 58 mm, REF 74121158 (b) Size 56 mm, REF 74123156
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Melissa's Spicy Edamame: Lightly seasoned with Japanese Chile and Sesame Oil. 7 oz. (1.98g) Keep Refrigerated UPC:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.World Variety Produce Inc.
FDA (openFDA food enforcement)
Reported Jun 20, 2018
lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego Inc. dba Immunalysis Corporation
FDA (openFDA device enforcement)
Reported Jun 20, 2018
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
37 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Meijer Dark Chocolate Covered Almonds, 18 ounces, packed in a Clear plastic container, 12 containers per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meijer, Inc. #816 - Grand River Packaging
FDA (openFDA food enforcement)
Reported Jun 20, 2018
Milk Chocolate Covered Fudge Bites, 3.75oz, PET Pouch, 12 packages per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morley Candy Makers, Inc.
FDA (openFDA food enforcement)
Reported Jun 20, 2018
Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Century Snacks LLC
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.