Recalls distributed in Rhode Island
These notices name Rhode Island 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.
1,557 stored notices name Rhode Island, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Rhode Island too — those are in the archive.
Reported Feb 12, 2014
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems. The Precision 500D R&F X-ray System…
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)
Reported Jan 29, 2014
ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Healthcare It
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Sandel Medical Industries LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 8, 2014
VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2014
Stuffed Foods Asiago Risotto Bites; UPC 850821-00301
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stuffed Foods LLC
FDA (openFDA food enforcement)
Reported Jan 1, 2014
OrthoPediatrics ACL Reconstruction System is a pediatric and small stature adult ACL reconstruction system containing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Jan 1, 2014
Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Aunt Jemima(R) HOMESTYLE FRENCH TOAST, 6 COUNT, NET WT. 12.5 OZ (354 g), UPC Code: 019600057703
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pinnacle Foods, LLC
FDA (openFDA food enforcement)
Reported Dec 25, 2013
Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg, 50 discs per cartridge, 5 cartridges…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Remel Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Nature's Way, UPC 33674149263, Alive Whole Food Energizer with Iron, 60 Tabs 20009807; Nature's Way, UPC 33674149270,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schwabe North America, Inc.
12 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 25, 2013
Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2013
Tuna Salads- packaged in: 7 oz., 12 oz., 5 lb.10 lb and 30 lb containers Sold under the labels: Boston Salads and the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Salads & Provisions Co., Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
Mediterranean Olives: Calcidica Sweet, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ocean State Jobbers, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
Woodstock Frozen Organic Pomegranate Kernels are sold in 8 oz. (227 gram) re-sealable plastic pouches with the UPC 0…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Scenic Fruit Co.
FDA (openFDA food enforcement)
Reported Nov 27, 2013
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Carestream Vue PACS; VIRTUAL ACCESS SOFTWARE, WORKGROUP The CARESTREAM PACS is an image management system whose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health Inc.
49 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Extended Phenytoin Sodium Capsules, USP, 100 mg, 1000 CAPSULES, Rx only, amneal PHARMACEUTICALS label, NDC 65162-212-11…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amneal Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Nov 13, 2013
Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids, or in various kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre; 15248C-22/25 The Regional Anesthesia family of products is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
VitreaCore¿ software. Versions subject to the limitation: 6.0, 6.1, 6.2, 6.3 (except 6.3.1 ), 6.4 (except 6.4.4 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vital Images, Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2013
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
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.