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 48,100 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Dec 13, 2023

Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w

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

Auris Health Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 13, 2023

BAPS SHAYONA Anjir Roll Sweet rolls made from fig and nut filling Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047…

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

BAPS Shayona

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 13, 2023

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

Freedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm…

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

Ihb Operations B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation

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

Liberty Medical Solutions, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

RANDOX Total Bilirubin.

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

Randox Laboratories Ltd.

FDA (openFDA device enforcement)

Food

Reported Dec 13, 2023

Whole cantaloupe, Brand name Malichita 11 count carton, 8 count carton, 9 count carton, 15 count carton d. Container…

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

Sofia Produce, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 13, 2023

EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.

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

Staar Surgical Company

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.

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

Stanbio Laboratory, LP

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176

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

Thor Photomedicine Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 6, 2023

BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

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

Becton Dickinson Infusion Therapy Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 6, 2023

Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646

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

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Food

Reported Dec 6, 2023

Breakfast Sandwich Bacon Egg & Cheddar Croissant Net Wt. 5.25oz (149g) UPC:766375253051. Packaged in clamshell…

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

The Coastal Companies dba Hearn Kirkwood

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

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 Nov 29, 2023

Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly SUB-00434 with foot pedal CUS-00226 Rev. K…

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

Convergent Dental

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…

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

SunMed Holdings, LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…

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

Beckman Coulter Biomedical Division

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051

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

Physio-Control, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 22, 2023

Takumi brand frozen tuna ground meat, raw but ready to eat, vacuum packaged units in fiber boxes, net wt. 11 lbs. per…

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

Tokai Denpun USA Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 15, 2023

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.

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

Abbott Laboratories

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

Novum IQ Syringe infusion system, Product Code 40800BAXUS

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

Baxter Healthcare Corporation

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.