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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 Jul 27, 2022

Hobbs Medical Polypectomy Snare, Catalog No. 7202

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

Hobbs Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip

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

LumiraDx

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate…

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036…

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

Synapse Biomedical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…

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

Cordis US Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

AquaBplus Water Purification System, Part Number 24-2000-0, AquaBplus 2500 - Typ USA (G02040108-US), AquaBplus 2000 -…

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

Fresenius Medical Care Holdings, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2022

GOODMAN GLUTEN FREE; Vegan Apple Pie, Fully Baked 16.4 oz, paperboard box; INGREDIENTS: Apples, Potato Starch, Palm…

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

Goodman Food Products LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 20, 2022

Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO)

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

Isopure Corp.

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2022

Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible…

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

J & M Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 20, 2022

Market Day Krabbycakes, Item 3320, Net Wt. 40 oz. (2.5 lbs.) 1.13kg. Item Number 803320R. UPC 51497 14360. Light panko…

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

Market Day Local Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

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

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC,…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Ventana HE 600 System, automated slide preparer, for use in laboratories.

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

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

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

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

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

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD intended for the enumeration of circulating tumor cells (CTC) of…

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

Menarini Silicon Biosystems

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and…

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 Jul 6, 2022

DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and…

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

Changzhou Biomet Medical Devices Co., Ltd.

FDA (openFDA device enforcement)

Food

Reported Jul 6, 2022

PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWAGANDHA PER 12 FL OZ STRAWBERRY CUCUMBER FLAVORED SPARKLING…

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

Independent Beverage Company LLC

FDA (openFDA food enforcement)

Food

Reported Jul 6, 2022

Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz. packed in clear plastic non-flexible package UPC 0 74641 00044 6…

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

Stellex/CF Houston, LLC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 6, 2022

Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797

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

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the…

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

Wright Medical Technology, Inc.

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.