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.
2,088 stored notices name West Virginia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.
Reported Feb 10, 2021
FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Feb 10, 2021
Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
32 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Weis Quality Cookies and Cream Ice Cream (48oz). Packaged in a squround paper container with a UPC of 041497-01253.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Weis Markets, Inc., Ice Cream Division
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 27, 2021
ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Penumbra Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 20, 2021
All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Jan 13, 2021
HRV Carrot.Cubes 1/20LB/HRV DCD Cartos 1/20LB - bag in box product in a corrugated case; IQF Cartotte Cubes 3/8"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bonduelle Canada Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 6, 2021
cobas pro integrated solutions -cobas c 503, Analyzer, chemistry (photometric discrete), for clinical use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Dec 30, 2020
42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
MAC VU360, Electrocardiograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 16, 2020
On the Go Sweet & Salty Trail Mix
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kanan Enterprises Inc.
FDA (openFDA food enforcement)
Reported Dec 16, 2020
Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
HomeChef Meal kit:One-Sheet Pretzel-Crusted Chicken with roasted broccoli and honey mustard..31.0 OZ (1 LB 15 OZ) 879g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 16, 2020
ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
FDA (openFDA device enforcement)
Reported Dec 9, 2020
CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 9, 2020
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
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.