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 Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2016
The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Ultrasonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son, New Bedford, MA UPC Code:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sid Wainer And Son
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jun 22, 2016
Oasis Foods Canola Fry Shortening, Net Wt. 35 LB (15.88), Distributed by: Oasis Foods, Inc. Hillside, NJ 07205, UPC 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oasis Trading Co., Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 22, 2016
The XN-Series modules (XN-10, XN-20) are quantitative multi-parameter automated hematology analyzers intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex Corporation
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Honest Kids-Super Fruit Punch, Organic Juice Drink, 59 fluid oz. bottle, 006 57622 41273 7, Honest Tea, Inc., 4827…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coca-Cola Company (The)
FDA (openFDA food enforcement)
Reported Jun 15, 2016
Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Novation Ceramic AHS Cluster-Hole Shell, Plasma Coated, 54mm, O.D. (Acetabular Cup), Catalog Number 140-01-54; For use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
RayStation Therapy Treatment Planning System Stand-alone Software 3.0, 3.5, 4.0, 4.5 and 4.7., designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 1, 2016
3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diamedix Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumenis Ltd.
FDA (openFDA device enforcement)
Reported May 25, 2016
Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Msu Dept Of Fd Sci Dairy Plant
FDA (openFDA food enforcement)
Reported May 25, 2016
COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unfi
FDA (openFDA food enforcement)
Reported May 18, 2016
Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 11, 2016
TCM CombiM Modules 903-111
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported May 11, 2016
Diced Red Potatoes, hand labeled: "Potato, Red Dice, 40# 3/4 large"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Specialty Produce Corporation
FDA (openFDA food enforcement)
Reported May 4, 2016
3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported May 4, 2016
Bliss French Vanilla Ice Cream 64oz Product Code: 51051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bliss Bros Dairy, Inc.
21 more products in this recall
FDA (openFDA food 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.