All recall categories

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.

3,277 stored notices name South Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.

Medical devices

Reported Jul 16, 2014

Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jul 16, 2014

Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…

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

Oregon Freeze Dry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…

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

Global Cooling Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2014

Physique Enhancing Science ALPHAMINE, Powerful Thermogenic Powder, DIETARY SUPPLEMENT Net Wt. 8.9 oz (252 g). Raspberry…

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

Physique Enhancing Science

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)

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

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

Philips/Children's Medical Ventures Smart Monitor 2 Professional Series infant apnea monitor.

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

Childrens Medical Ventures

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

Spacelabs Healthcare Ventilator Flexport Interface, Model 90436A-07

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

Safety glasses made with "Rage" frames manufactured between February 20, 2014 and February 25, 2014. The color of the…

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

Wal Mart Stores, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2014

Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use.

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2014

Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management application that is…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is…

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

Aesculap, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive (BioGlue) is indicated for use as an adjunct to…

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

CryoLife, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser software. LAP isocenter marking control software. Laser…

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

Lap

FDA (openFDA device enforcement)

Food

Reported Jun 11, 2014

Greens+ Vegan Crisp Bars - Dark Chocolate Almond Blueberry in 1.4 oz packages.

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

Orange Peel Enterprises, Inc.

2 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.