All recall categories

Recalls distributed in North Carolina

These notices name North 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.

4,689 stored notices name North Carolina, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Mar 25, 2020

Boston Scientific, LATITUDE Programming System, Model 3300 - Product Usage:The Boston Scientific LATITUDE Programming…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device 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)

Medical devices

Reported Mar 25, 2020

LEGION PS High Flex XLPE size 5-6 9mm Articular Insert

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe; STERILE R, Product Code: 359100, Dimensions:…

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

Xtant Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102…

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

ARJOHUNTLEIGH POLSKA Sp. z.o.o.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…

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

Cardinal Health 200, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

PREMIUM SELECTIONS BANANA PUDDING ICE CREAM NATURALLY & ARTIFICIALLY FLAVORED 1.5 QUART (1.42 L) KEEP FROZEN CONTAINS:…

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

Harris Teeter Supermarkets, LLC dba Hunter Farms

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

Randox Laboratories Ltd. Catalogue Number CQ5052, Lot Number 4244CK (relabeled as Response Biomedical Catalogue Number…

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

Response Biomedical Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For in vitro diagnostic use, Product Code:…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical…

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

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5…

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

Bard Peripheral Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

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

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Driscoll's Raspberries- 6 oz. clamshell container 12 x 6 oz. per crate and 6 x 12 x 6 oz. (2 - 6 oz. attached…

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

Driscoll's Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Elecsys CA 19-9, Cat. No. 07027028190 - Product Usage: the product is an immunoassay for monitoring and management of…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009

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

Seca

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

chef's recipe MUSHROOM BARLEY SOUP NET WT 16 OZ (1LB) 454g PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATTHEWS, NC…

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

Bakkavor Foods USA Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 4, 2020

C&H Pure Cane Sugar Golden Brown, 32 oz (2 LB) plastic bag, UPC 015800090038, Lots 50042 (Best By Jan 21, 2022) & 50043…

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

Domino Foods Inc.

7 more products in this recall

FDA (openFDA food 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.