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.
4,767 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,868 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Jul 4, 2012
Formula Shaver Handpiece (with buttons); Formula 180 Shaver Handpiece (with button) Rx only, Made USA.: Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Endoscopy
FDA (openFDA device enforcement)
Reported Jul 4, 2012
Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12 GAUGE BLUE NEEDLE RECTANGULAR FLANGE, 6" (15…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
19 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2012
Reggano, Linguine and Parmesan Pasta Entree, NET WT 4.8 OZ(136g), UPC 4149813345, Distributed by ALDI Inc., Batavia, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TreeHouse Foods, Inc. / Bay Valley Foods
8 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 4, 2012
Bigliani/Flatow The Complete Shoulder Solution Trabecular Metal Glenoid Instrument Drill with Stop, 6 mm; the products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2012
Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2012
KERRY, 4 CHEESE SEAS 30506103, CONTAINS MILK, Net Wt 50 Lb (22.68 Kg), Item Number 30506103.465
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry Foods
61 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 27, 2012
Granadaisa whole Oysters, Net WT. 8 oz (225 grams); Packed For King Seafoods Inc. PO BOX 107, Mount Holly, NJ USA 08060…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.King Seafoods Inc.
FDA (openFDA food enforcement)
Reported Jun 27, 2012
Oskri, Peach Granola, Gluten Free, Nut Free, Dairy Free, Vegan, Halal, Kosher, Ingredients: Buck Wheat , Peaches 20%…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oskri Organics Corp.
FDA (openFDA food enforcement)
Reported Jun 27, 2012
Lipitor (Atorvastatin calcium); 40 mg, 30 TABLETS, Rx only, Repacked & distributed: Physicians Total Care, Inc., Tulsa…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physicians Total Care, Inc.
FDA (openFDA drug enforcement)
Reported Jun 27, 2012
SARNS HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 FR) 00 WITH 3/8" CONNECTOR, 7.5" (19 CM) LONG. The Sarns High Flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2012
AlsoSalt Sodium Free Butter flavored Salt Substitute, 2.5 oz. bottle
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diversified Natural Products, Inc.
FDA (openFDA food enforcement)
Reported Jun 20, 2012
Polar Whole Boiled Oysters, 8 oz. net weight, 12 cans/carton.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Milky Way Intl Trading Corp.
FDA (openFDA food enforcement)
Reported Jun 20, 2012
The Brilliance iCT and iCT SP are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 20, 2012
Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 30-count tablets per bottle (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physicians Total Care, Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2012
T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
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.