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 48,123 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Jul 11, 2018

26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 11, 2018

WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR…

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

Caito Foods Service, Inc.

25 more products in this recall

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

Reported Jul 11, 2018

Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135

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

Terumo Medical Corp.

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 6, 2018

Tillamook Country Smoker, LLC Retira Productos De Carne Seca (Jerky) De Res Listos Para Consumir Debido A Un Error De…

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

Tillamook Country Smoker, LLC

USDA FSIS

Food

Reported Jul 4, 2018

Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as…

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

Absonutrix

FDA (openFDA food enforcement)

Medical devices

Reported Jul 4, 2018

HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model…

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

Cenorin, LLC

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2018

Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case

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

Golden Star Wholesale Inc.

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

Reported Jul 4, 2018

RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

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)

Food

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)

Medical devices

Reported Jun 27, 2018

CritiCore Automated Urine Output and Temperature Monitor

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

VNS Therapy Programmer, Model 3000, v1.0 System

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

Cyberonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The CARESCAPE R860 ventilator is designed to…

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

Datex-Ohmeda, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…

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

Draeger Medical, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

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)

Medical devices

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)

Medical devices

Reported Jun 27, 2018

Part no. 690.375, Graphic Case F/6.5mm & 7.3mm Combined Cannulated Screw Set

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

Synthes (USA) Products LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2018

Nitinol Staple, Elastic Staple Large-Asymmetrical, Sterile R, Model #: a) ES-18x15x17; b) ES-18x17x19

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

TriMed Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control…

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

Alere San Diego Inc. dba Immunalysis Corporation

FDA (openFDA device enforcement)

Medical devices

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)

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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.