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.

Medical devices

Reported Apr 15, 2020

BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.

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

Biomet, Inc.

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable…

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

James Leckey Design Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Lindt & Sprungli (USA), Inc.; Excellence 85% Cocoa Dark Chocolate; Net WT 3.5OZ (100g)

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

Lindt & Sprungli (USA), Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2020

ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

ARTISTE MV System Model #8139789 with Digital LINAC Systems Control Console Software Versions 6, 7, 9, 13

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

PRIVATE SELECTION FROZEN BERRY MEDLEY in 16 oz. (10 bags per case) and 48 oz. bags (6 bags per case). UPC: 0001111079120

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2020

Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2020

BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care of a healthcare professional, Gentell…

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

Gentell, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Philips V60 Ventilators with Power Management PCBA part number 1055906

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

Respironics California, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only,…

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

Stryker Neurovascular

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144

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

Abbott Diabetes Care, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

LN 3R70-01; software version 2.6.2 and earlier. The software is used with the Alinity i (LN 03R65-01) processing module…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

American Classic Snack Company Sweet Bourbon Crunchers Pretzels in 8 oz. bags, 12 bags per case.

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

American Classic Snack Co., LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…

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

Bard Peripheral Vascular Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is…

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

Hill-Rom Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

Clover seed in 50 lb. woven poly bags, 40 bags to a pallet.

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

International Sprout Holding Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope

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

Karl Storz Endoscopy

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.

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

Medline Industries Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

Whole Foods Market Green Chile Chicken Tamale served as a Family Meal, Chef's Case, Packaged, Frozen and on he hot bar…

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

Whole Foods Market

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…

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

CME America, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044

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

Dreyers Grand Ice Cream, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…

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)

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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.