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 48,132 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Apr 2, 2014

HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage:…

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

Thoratec Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 2, 2014

DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care…

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

Velocity Medical Solutions, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Reusable Clip Applier Manufactured by AtriCure, Inc., 6217 Centre Park Drive, West Chester, OH 45069. The Reusable Clip…

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

Atricure Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens, FL 33410 USA 1-800-342-5454***EDAZ , EDAZx…

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

Biomet 3i, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

DeRoyal(R) LIMB HOLDERS, COTTON ADJUSTABLE, UNIVERSAL, REF M2017 Product Usage: Limb holders are intended for mildly to…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

GE Healthcare Optima CT580/Discovery CT590RT scanners running software version 13BW16.3. The Discovery CT 590 RT and…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 26, 2014

High Mowing Organic Sprouting Seeds Ancient Eastern Blend , 4 oz. resealable plastic bag UPC Code: 872724005445

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

High Mowing Organic Seed

FDA (openFDA food enforcement)

Medical devices

Reported Mar 26, 2014

Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a…

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

Philips Medical Systems North America Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated…

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Sarns Malleable Dual-stage Venous Return Cannulae, 28/38 Fr with 1/2" connector, 14.5" (37 cm) long The Sarns Malleable…

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

Terumo Cardiovascular Systems Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT

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

Zimmer, Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

bioMerieux PREVI Isola System (General purpose,microbiology, diagnostic Medical Device), (REF 29500/29500R),…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Navigator Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave…

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

Biomet 3i, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588.…

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

Clarity Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis IHC PR Breast Tissue Manual Read of Digital…

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

Leica Biosystems Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Cannabinoids DAU Calibrator Control Level 1 (37.5 ng/mL) This solution is prepared from non-sterile urine and should be…

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

Lin-Zhi International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with…

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

Smith & Nephew Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…

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

Smiths Medical ASD, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

VERIFY¿ SixCess 270FP Challenge Pack, STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060, 440-354-2600. The…

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

Steris Corporation

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2014

Whole (round) Tomatoes packed in cardboard boxes of 20 and 25 lbs each.

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

Big Red Tomato Packers, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2014

All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…

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

Elekta, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On-…

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

GE Healthcare, LLC

1 more product in this recall

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.