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 Dec 31, 2014
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Halyard Health
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Ceramic Femoral Head. Intended for use in total hip arthroplasty applications to replace the articular surface of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2014
KOZY SHACK SIMPLY WELL CHOCOLATE, NET WT 4 OZ. Product packed in brown carton box, 48 individual units x 4 OZ. Keep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kozy Shack Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
Mammomat Inspiration system: Product Usage: mammography exams, screening, diagnosis, and stereotactic biopsies under…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Dec 3, 2014
The J700 Floor Mounted Tube Stand (FMTS) is intended to support and position the diagnostic x-ray tube housing assembly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Summit Industries Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 19, 2014
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Prescription eyeglass safety lenses. Vision correction
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eyemart Express Ltd.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric handpiece is packaged within a foam bag inside of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4";…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Briggs Medical Service Company d.b.a. Mabis
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Laksell Gamma Knife Perfexion
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Family Gourmet Long Grain Enriched White Rice in 32 oz. clear plastic bags (SKU: 1218898) and 80 oz. clear plastic bag…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Family Dollar Stores - NC Distribution Center
FDA (openFDA food enforcement)
Reported Nov 5, 2014
The GemStar Power Supply is an accessory for the GemStar Infusion Pump. It is a two piece assembled switching power…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medartis, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage: The ACCU-CHEK Combo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Ciprofloxacin 500 mg tablets, 20 count bottle, Rx only, Packaged by Aidarex Pharmacecuticals LLC, MFG: Unique…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aidarex Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Oct 29, 2014
Suction canisters labels as follows: 1) DeRoyal(R) SUCTION CANISTER, 1000cc, SEMI-RIGID, REF 71-6510, NON-STERILE, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Wild'erb Seasoning 2 oz and 4 oz plastic jars; seasoning contained less than 1% sassafras leaves.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ohio Valley Herbal Products, Inc.
1 more product in this recall
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.