Recalls distributed in North Carolina
These notices name North Carolina 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.
4,767 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,868 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Sep 26, 2012
Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW STEMS AND 12/14 FEMORAL COMPONENTS ONLY CO-CR, REF 71352112, Smith…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Spence & Co Ltd brand 8oz Smoked Salmon Trim
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spence & Co., Ltd.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 26, 2012
Watermelon, labeled IT'S WATERMELON TIME!, Produce of USA, Seedless, #4032.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tunnel Farms
FDA (openFDA food enforcement)
Reported Sep 26, 2012
Infinity¿ sampling device, Cytology Brush, United States Endoscopy Group, Inc., 5976 Heisley Road, Mentor, OH 44060 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used by qualified medical personnel for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Sterile Empty Vial and Injector (30mL PCA vial), Rx only, One/List No. 6021-03, Hospira, Inc., Lake Forest, IL 60045.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira, Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Crown Program BK Fresh Apple Slices, 2 oz On or before August 13; no upc code
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 12, 2012
AmeriWater MRO Dialysis RO+ System, AmeriWater 1303 Stanley Avenue, Dayton, OH 45404 (800) 535-5585 www.AMERIWATER.com.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AmeriWater Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
BD GeneOhm MRSA ACP Assay Catalog #441637, box 48 tests labeled in part***GeneOhm Sciences Canada, Inc., 2555 boul, du…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2012
OPTETRAK LOGIC TIBIAL INSERT POSTERIOR STABILIZED***Match Component Colors 6 YELLOW, 11mm, Use with LOGIC Femoral and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Fresh Express Hearts of Romaine Crunchy and Sweet 100% Hearts of Romaine Lettuce. 10 oz. plastic bag UPC 71279 26102.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorporated
FDA (openFDA food enforcement)
Reported Sep 12, 2012
syngo(R) Lab Data Manager and syngo(R) Lab Process Manager, all versions. This device is classified as a data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Siemens Mobilett Mira. Mobile X-Ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Trader Jose's, Mild Salsa, 16 ounce (1 lb) 454g), in clear rigid plastic containers with snap on lids.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simmering Soups Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 12, 2012
VersaTREK Windows Software, Version 5.4.3 is a component of the VersaTrek System. The Software CD will be individually…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Trek Diagnostic Systems
FDA (openFDA device enforcement)
Reported Sep 5, 2012
16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bard Access Systems
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Whole Fresh Cantaloupe, PLU# 4319, Burch Farms, Faison, NC 28341. On 8/2/2012 the recall was expanded to include…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Burch Farms
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 5, 2012
Dole Italian Blend; Romaine, Radicchio; 10 oz plastic bag (283g); UPC:7143000819. Dole, Monterey, CA 93942.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Sep 5, 2012
V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. d.b.a. Mindray North America
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots 502058002 and 501318002 The Stratus(R) CS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2012
syngo Imaging XS. Radiological image processing system.
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 Sep 5, 2012
Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory Packs (also commonly known as convenience…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SRI Surgical
FDA (openFDA device enforcement)
Reported Sep 5, 2012
QKC1692E The QKC1692E Quick Connect device connects endoscopes to the sterilization tray for C1220E liquid chemical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
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.