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 Feb 26, 2020
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suja Life LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 26, 2020
OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Bakers Corner All Purpose Flour in 5 lb. bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Adm Milling
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 19, 2020
FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
48 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market America Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon Vinaigrette; Baby Spinach, Hard Boiled Eggs, Monterey…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ready Pac Foods, Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz canister, DISTRIBUTED BY FOODHOLD USA, LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sugar Foods Corporation
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Almark Foods, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Cocoon Convective Warming System, Product Code: CWS4000 (110V).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Care Essentials Pty., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ducktrap River
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
FDA (openFDA device enforcement)
Reported Feb 12, 2020
da Vinci Xi Surgical System Surgical System, IS4000, 00886874114216 - Product Usage: used with an endoscope, surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Fresh Grab Ham & Swiss on Pretzel Sub Bun, 6 oz., UPC: 612510001028
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
31 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
PediaLift Access Device, Device Identifier: B751PDLFT0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PediaLift LLC
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.