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 Jun 5, 2013

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

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

Nephron Pharmaceuticals Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…

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

Orthovita, Inc., dba Stryker Orthobiologics.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

MyRay RXDC dental unit x-ray unit

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

Cefla Dental Group

FDA (openFDA device enforcement)

Food

Reported May 29, 2013

Krinos TAHINI ground sesame seeds, 1) Net. Wt. 1 lb (454g) in glass jars with gold lids packed 12 jars per case - UPC…

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

Krinos Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2013

Ref: VP1600 HD Still Capture System ConMed Linvatec . Captures, stores and transfers images generated by a medical…

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

Linvatec Corp. dba ConMed Linvatec

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…

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 May 22, 2013

AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control System is used to treat urinary incontinence due to…

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

American Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The gloves are designed to resist sticks and…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. Product Usage: The catheter…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses. The Vistakon (etafilcon A) Soft (hydrophilic)…

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

Johnson & Johnson Vision Care, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 22, 2013

Add a Scoop by Smoothie Essentials; Probiotic; Supports Digestive Health, dietary supplement; Net Weight: 1 lb (464g)…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Juice Bar Solutions

FDA (openFDA food enforcement)

Food

Reported May 22, 2013

Adobo sin pimienta (Adobo without pepper) in 5 oz, 14 oz, and 32 oz

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

Lisy Corp.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 15, 2013

Presource PBDS, Gyn Laparoscopy Kit, Circulator

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

Cardinal Health, Medical Products & Services

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD…

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

Karl Storz Endoscopy America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…

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

Olympus America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

Synthes Radial Head Prosthesis: Trial Radial Head Elbow joint prosthesis: Synthes Radial Head Prosthesis System is a…

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

Synthes USA HQ, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…

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

Advanced Sterilization Products

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis…

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT750HD. Intended to…

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries Model number: HT70 and HT70 Plus. The…

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

Newport Medical Instruments Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case The NxStage PureFLow-B Solution is…

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

NxStage Medical, Inc.

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.