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 48,132 notices were distributed nationwide, so they reach Ohio too — those are in the archive.
Reported Feb 26, 2014
Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device with wheels that is intended for medical purposes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Standing Company
FDA (openFDA device enforcement)
Reported Feb 19, 2014
Boston Scientific, 2.5mm Coyote" OVER-THE-WIRE PTA Balloon Dilation Catheter, UPN# H74939186251210, Catalog #…
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 Feb 19, 2014
BrainLAB's VectorVision spine is intended for use as an intraoperative image-guided localization system for minimally…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Feb 19, 2014
Medtronic GRAFTON (R) DBM, Flex 2.5cm x 10cm, REF T42100, Rx only, STERILE A, QTY: 1 EA, Medtronic Sofamor Danek, USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2014
enGen Track System with enGen Select v5.0 with autoverification enabled Product The VITROS 5,1 FS Chemistry System with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2014
GEMINI TF Big Bore PET/CT, Computer Tomography System, Philips Healthcare System, Cleveland, OH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2014
The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urinalysis. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex America, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
IMPAX RIS QDOC 5.8
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Corp.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
FDA (openFDA drug enforcement)
Reported Feb 12, 2014
XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
***REF 186-01-08***InteGrip ACETABULAR AUGMENT***SMALL 8mm. Use with 48/50mm Shell.***EXACTECH, Gainesville, FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number: 10-1357 (Generator assembly), 40-404-1(as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Advanced Energy, LLC
FDA (openFDA device enforcement)
Reported Feb 12, 2014
3.5mm Locking Cortical Bone Screw, T15 Hexalobe, Self Tapping, 20mm Part No. 00-0903-2620 OrthoPediatrics Pediloc"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
Diagnostic imaging systems (GEMINI LXL Model #882412, TruFlight Select Model #882438, GEMINI TF PET/CT16 Model #882470,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
LOCATOR¿ Implant Attachment System. The LOCATOR¿ Implant Attachment System is a universal hinge, resilient attachment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zest Anchors LLC
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Simplexa Flu A/B & RSV Direct assay, Model MOL2650. The Focus Diagnostics Simplexa Flu A/B & RSV Direct assay is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Focus Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Intended to produce cross-sectional images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Number H965450140,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Navilyst Medical, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Brilliance iCT, Brilliance 64 and Brilliance Big Bore The Brilliance iCT, Brilliance 64 and Brilliance Big Bore are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only. Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Watson Laboratories Inc.
FDA (openFDA drug enforcement)
Reported Jan 29, 2014
BD GeneOhm Cdiff Assay, Part #441401, containing Lysis Kit sample buffer tubes, 200 tests/kit; labeled as ***GeneOhm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Jan 29, 2014
DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2014
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Churchill Medical Systems, 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.