Recalls distributed in West Virginia
These notices name West Virginia 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.
2,092 stored notices name West Virginia, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.
Reported Jun 12, 2013
AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Corp.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nephron Pharmaceuticals Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aaron Industries Inc.
FDA (openFDA drug enforcement)
Reported May 29, 2013
Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported May 15, 2013
KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
FDA (openFDA device enforcement)
Reported May 15, 2013
Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus America Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported May 8, 2013
Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
BUFFALO TRACE BOURBON FLAVORED CARAMEL SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g, PRODUCED BY: APPLECREEK ORCHARDS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Buffalo Trace Distillery
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 1, 2013
Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Biomedical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2013
Sirtex SIR-yttrium 90 microspheres (Radionuclide); SIR-Y001. Indicated for the treatment of unresectable metastatic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sirtex Medical Limited
FDA (openFDA device enforcement)
Reported May 1, 2013
Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Term Monitoring system (Models HSYS-REC-WD, HSYS-REC-WT;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stellate Systems
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Industries Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Intellispace Portal (ISP) Philips Medical Systems (Cleveland), Inc., IntelliSpace Portal (ISP) is a multimodality (CT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and B) labeled in part: ***GE Healthcare 8880 Gorman…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Giant Eagle Lotsa Chocolate Chip Cookies
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Giant Eagle
FDA (openFDA food enforcement)
Reported Apr 17, 2013
Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the determination of the activated partial thromboplastin time…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Flexible Grip which is part of the Synthes Universal Nail System. Indicated for the conventional (non-locking)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, 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.