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.
2,055 stored notices name West Virginia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.
Reported Jun 28, 2017
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monfitello
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Spinach Sold under the brand names of Harris Teeter Farmers Market, 10 oz bag, PROUDLY DISTRIBUTED BY: HARRIS TEETER,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Horton Fruit Co. Inc.
FDA (openFDA food enforcement)
Reported Jun 14, 2017
Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 9, 2017
CC Kitchens, LLC Retira Productos De Ensalada De Carne Y Aves Debido A Posible Contaminación Con Listeria
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Jun 7, 2017
Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Scale Mfg Co.
FDA (openFDA device enforcement)
Reported Jun 7, 2017
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Jun 2, 2017
P&S Bakery, Inc. Recalls Pepperoni Product Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.P&S Bakery, Inc.
USDA FSIS
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 10, 2017
Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Guggisberg Cheese Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported May 3, 2017
Season's Choice Garden Fresh Sweet Peas, Net Wt 16 oz (1lb) 454g, Keep Frozen. UPC 41498-164294.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lakeside Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ashers Chocolates/Lewistown, Inc.
86 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien Medtronic
FDA (openFDA device enforcement)
Reported Apr 26, 2017
GUGGISBERG NATURAL CHEESE COLBY INGREDIENTS: Pasteurized Milk, Cultures, Salt, Enzymes, Annatto Color 1 lb, 2 lb, 6 lb…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dutch Valley Food Distributors
11 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 19, 2017
LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nonna Foods
FDA (openFDA food enforcement)
Reported Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; Core-Mark Turkey & Garlic Mayo Item # 568207, Net wt. 5.5 oz;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
7 more products 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.