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 48,100 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.
Reported Sep 19, 2018
Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
128 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
VidiStar(TM) PACS & DICOM Viewer Software system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Healthcare Americas Corp. Informatics Division
FDA (openFDA device enforcement)
Reported Sep 12, 2018
McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and data processing.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Israel Ltd.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Virtus Pharmaceuticals Llc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 5, 2018
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Sep 5, 2018
FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Stryker Mako Vizadisc Knee Procedure Tracking Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Amlodipine/Valsartan/HCTZ 10mg/320mg/25mg Tablet, Rx Only (HDPE 90cc Bottles in cardboard trays) MFG Torrent Pharma…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported Sep 5, 2018
Cortisol Saliva Luminescence Immunoassay The IBL International Cortisol Saliva Luminescence immunoassay is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CAREstream Medical LLC
FDA (openFDA device enforcement)
Reported Aug 29, 2018
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare Japan Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liebel-Flarsheim Company LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salt & Straw LLC
FDA (openFDA food enforcement)
Reported Aug 29, 2018
TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag, and 4 oz., and 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teasource
FDA (openFDA food enforcement)
Reported Aug 29, 2018
Connecting Bolt, Model 14-442093
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Clarity Urocheck 10SG Urinalysis Strips, Model # DTG-10SG Product Usage: Clarity 10SG Urinalysis Reagent Strips (Urine)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clarity Diagnostics LLC
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Aug 22, 2018
1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, 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.