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 Jul 18, 2018
Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, SCS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2018
Reliance 1227 Cart and Utensil Washer/Disinfector, FW03101, FW03102, FW03S003 Product Usage: The Reliance 1227 Cart and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jul 18, 2018
Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water, packaged in a PET bottles with a plastic cap, Net Wt.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talking Rain Beverage Co. Inc.
FDA (openFDA food enforcement)
Reported Jul 11, 2018
ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ecolab Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Jul 11, 2018
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Single Chamber Temporary External Pacemaker, Model 53401
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 27, 2018
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kellogg Company
FDA (openFDA food enforcement)
Reported Jun 27, 2018
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Jun 20, 2018
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
37 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Century Snacks LLC
FDA (openFDA food enforcement)
Reported Jun 20, 2018
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
cobas e 801 immunoassay analyzer, cobas 8000 Modular Series The device is a fully automated, software controlled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device intended to be used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Part #: SAM XT-M, Model: Tactical Black or Military
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Seaberg Company Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Priano Rosso Pesto Sauce, 6.7oz glass jar
High riskUsing this product could cause serious injury, illness or death — stop using it now.BLM Products U. Vertriebsges
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic package with UPC 4770049011188.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Desly International Corp.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lake Michigan Distilling Co. LLC
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix, Inc.
19 more products 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.