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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.

Medical devices

Reported Mar 14, 2018

2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…

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

Synthes (USA) Products LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…

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

ConMed Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Agility with Integrity R3.2

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

Elekta Limited

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Ultrasound Transducer, Model Number: UST-5550-R, is used in conjunction with a diagnostic ultrasound system evaluation…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant, Catalog Number D-TAP-MAX7-7 Dental implants are…

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

Keystone Dental Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed…

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

Mobius Imaging, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 7, 2018

BNS WHEAT ROLLS ( Under the following Trade Names - Giant, Harvest Pride, Shoppers and Old Tyme )

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

Schmidt Baking Co., Inc.

25 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 7, 2018

Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381

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

Seggiano USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 7, 2018

Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…

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

Zimmer Biomet, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 28, 2018

Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth, Mary B's & Marshall.

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

Holsum Baking Company Warehouse

FDA (openFDA food enforcement)

Medical devices

Reported Feb 28, 2018

Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…

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

Pentax

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,…

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

Coblentz Distributing Inc. dba Walnut Creek Foods

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

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

GE Medical Systems China Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…

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

Zimmer Surgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2018

ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2018

AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed…

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

Brainlab AG

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2018

DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE

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

Zimmer Biomet, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2018

Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100…

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

Dollar General Corporation, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2018

Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…

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

Ormco/Sybronendo

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2018

ACCOLADE SR Pacemaker

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

Boston Scientific Corporation

23 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 24, 2018

Frozen Tuna Fillet Saku (Restaurant Supply Only); 22 lbs./2 x 5 kgs. Wild caught: Handline with Hook. Keep Frozen - 18…

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

H.I.G. Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jan 24, 2018

Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic,…

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

Owen Mumford USA, Inc.

1 more product 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.