Recalls distributed in South Carolina
These notices name South 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.
3,219 stored notices name South Carolina, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.
Reported Oct 8, 2014
GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumed International, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…
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 Oct 8, 2014
Siemens Ysio Max system The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is designed for use on patients who require…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 203, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Product is packaged in a cardboard box and labeled in part, "SOUTHERN HOME Mozzarella Sticks***CONTAINS: WHEY, MILK,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Great American Appetizers, Inc.
FDA (openFDA food enforcement)
Reported Oct 1, 2014
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pdg Product Design Group Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)]…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Peters Surgical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
No packaging. The device is a computed tomography scanner. Intended to provide corss sectional images of the human body…
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)
Reported Oct 1, 2014
Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidacare Corporation
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GF Health Products, Inc./d.b.a.Basic American Metal Products
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Clover, Crimson, Net Wt. 50 LB. PRODUCT OF USA, International Specialty Supply, 1011 Volunteer Drive, Cookeville, TN…
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holding Inc.
FDA (openFDA food enforcement)
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 24, 2014
Activia Lowfat Yogurt Blueberry 4 x 4oz, Form Fill Seal plastic cups.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Dannon Company, Inc. - Discovery & Innovation Center
FDA (openFDA food enforcement)
Reported Sep 17, 2014
The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE; the Airway Gas Option N-CAiO and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Sep 10, 2014
Lacteos Santa Martha Quesito Casero Fresh Curd Net Weight 12oz Distributed by Oasis Brands Inc., Miami FL 33192
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oasis Brands, Inc.
FDA (openFDA food enforcement)
Reported Sep 10, 2014
Roche cobas IT 1000 Product Usage: Intended Use: An electronic device intended to store, retrieve, and process…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2014
Organic Carob Powder, 1 lb., 20 lb., and 55 lb. bags Expiry date: 6/5/2015, UPC Code 803813-04429-8
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sunfood Superfoods
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.