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 Sep 19, 2018

da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…

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 19, 2018

Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280

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

Zimmer Biomet, Inc.

128 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens…

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

Alden Optical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD)

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 12, 2018

Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle

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

Virtus Pharmaceuticals Llc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 5, 2018

Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 5, 2018

equate High Performance Protein Shake: Chocolate, Naturally & Artificially Flavored, ready to drink; 11 FL OZ (325 mL),…

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

California Natural Products

FDA (openFDA food enforcement)

Medical devices

Reported Sep 5, 2018

Stryker Mako Vizadisc Knee Procedure Tracking Kit

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

Mako Surgical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…

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

CAREstream Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an…

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

Compass Health Brands (Corporate Office)

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

BEST TASTE BRAND SNACK GINGER SLICED, Net Weight 200g, 7 OZ, Distributed by; COUNTRY FAVOR., INC U.S.A; PRODUCT OF…

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

Country Favor Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…

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

GE Healthcare Japan Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend, Net Wt. 15 lbs (6 / 2.5 lb bags per case), UPC…

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

J R Simplot Co. Corporate HQ

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…

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

Liebel-Flarsheim Company LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag, and 4 oz., and 2…

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

Teasource

FDA (openFDA food enforcement)

Medical devices

Reported Aug 22, 2018

Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with…

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

Apollo Endosurgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath…

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

Arrow International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

20 cm (8") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer single use,…

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

ICU Medical de Mexico, S.A. de C.V.

19 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.