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.

3,219 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.

Food

Reported Nov 6, 2019

LUNCH BOX SANDWICHES CHICKEN SALAD; NET WT 4.5 oz (127G); MADE BY: GS Sandwich Co. Longs, SC 29568 843-399-2999; UPC 0…

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

Grand Strand Sandwich Company,Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

HYTEC Stop Solution (Allergy), 300ml bottle containing 1N sodium hydroxide solution, Part # 308051, sold separately or…

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

Hycor Biomedical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…

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

Pajunk GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Posey Connected Twice-As-Tough Cuffs

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

Tidi Products

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald instrument, List number 09H39-01. The firm…

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

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

IrriMAX Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic…

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

Mrs. Stratton's Salads, Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 30, 2019

Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…

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

Roland Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix. Packaged in 13 oz (380 g) sealed plastic bags with paper…

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

The Truck Farm, LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Oct 29, 2019

H&T Seafood, Inc. Retira Productos Siluriformes Sin El Beneficio De La Inspeccin

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

Recalling firm not stated

USDA FSIS

Food

Reported Oct 23, 2019

Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS…

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

Gullah Gourmet, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 23, 2019

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…

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

ICU Medical Inc.

21 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2019

Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the…

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

Roche Diagnostics Operations, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 23, 2019

Fentanyl Citrate USP, Active Pharmaceutical Ingredient, Spectrum Chemical MFG. CORP., Gardena, CA 90248 NDC…

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

Spectrum Laboratory Products

FDA (openFDA drug enforcement)

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Other states

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.