All recall categories

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.

Medical devices

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)

Medical devices

Reported Jan 29, 2014

Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, packaged 1 per box. Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Civco Medical Instruments Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2014

ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ge Healthcare It

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Leica Biosystems Newcastle Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2014

Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin), 40.8 g Methyl Acrylate Copolymer, 20 ml Methyl…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2014

Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe, 1.0ml 29g x 1/2 in Reference: 4429-1…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2014

IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill syringes from 0.5mL up to 11.5mL using mixing…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2014

VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2014

Diced Summer Slaw Salad Kit Fresh Food Manufacturing Company 10.5 lbs

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresh Foods Manufacturing Co.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2014

McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mckesson Information Solutions LLC

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2014

Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Quaker Foods and Snacks North America

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 1, 2014

Macaroni Reg CAD, Formula MA.50, Macaroni Salad, packaged: -7-Eleven Fresh to Go Macaroni Salad, 12/7-oz carton cases.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Reser's Fine Foods, Inc.

212 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2014

Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ziehm Imaging Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2013

VITROS CA 125 II Calibrators For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, VITROS 3600…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2013

Nature's Way, UPC 33674149263, Alive Whole Food Energizer with Iron, 60 Tabs 20009807; Nature's Way, UPC 33674149270,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Schwabe North America, Inc.

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2013

Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2013

AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile, wheeled transportation unit utilized to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

FDA (openFDA device enforcement)

Drugs

Reported Dec 11, 2013

17-P 1ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Main Street Family Pharmacy, LLC

298 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 4, 2013

Baxter, VIAL-MATE Adaptor, 2B8071, Rx Only, STERILE R, Baxter Healthcare Corporation, Deerfield, IL 30015 USA The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2013

Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kraft Foods Group

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2013

2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recess 12 MM Fixation of fractures, osteotomies, nonunions,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes USA HQ, Inc.

15 more products in this recall

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.