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.

Food

Reported Sep 23, 2020

Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.

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

Blue Apron Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2020

FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to Rack Module…

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

Inpeco S.A.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2020

The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…

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

Life Technologies Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2020

NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…

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

Novarad Corporation

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2020

Wegmans Vanilla Trifle; 9oz; UPC 7789080600

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

Wegmans Food Markets, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 16, 2020

BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…

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 Sep 16, 2020

Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.

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

Hellofresh US

FDA (openFDA food enforcement)

Medical devices

Reported Sep 16, 2020

Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

Merge PACS

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2…

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

MicroPort Orthopedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Food

Reported Sep 16, 2020

Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz (1219g) Packed for Whole Foods Market PLU 41070 packaged…

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

Whole Foods Market

FDA (openFDA food enforcement)

Meat & poultry

Reported Sep 11, 2020

Cher-Make Sausage Company Recalls Fully Cooked Meat Sausage Products Due to Misbranding and an Undeclared Allergen

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

Cher-Make Sausage Company

USDA FSIS

Medical devices

Reported Sep 9, 2020

BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

Parvovirus B19 IgG EIA kit Part No. V519IGUS

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

Diasorin Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…

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

Stimwave Technologies Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical…

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

Teleflex Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…

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

Biosense Webster (israel), Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…

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

Karl Storz Endoscopy

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 2, 2020

Wegmans Chicken Cutlet; by the lb, in a meal or in a 22 oz. Family Pack; "Heating Instructions: Oven-Preheat to 400…

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

Wegmans Food Markets, Inc.

22 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 2, 2020

Whole Foods Market Buttermilk Biscuits, 4pk NET WT 1lb 0 oz PLU: 30561 packaged in plastic clam shell

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

Whole Foods Market

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.