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 May 10, 2017
Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
Apple Cider with Potassium Sorbate, packed under the following labels: RUDY'S BLEND APPLE CIDER; 1 GAL. (3.78L), UPC: 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bevovations, LLC dba New England Apple Products Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ashers Chocolates/Lewistown, Inc.
86 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 19, 2017
ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2017
LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nonna Foods
FDA (openFDA food enforcement)
Reported Apr 19, 2017
Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 5, 2017
AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 5, 2017
JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Hitachi Oasis MRI System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Whole Foods Spinach Orzo Salad Our Chef's OWN, sold by weight PLU:beginning with 61159
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Food Market
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 22, 2017
BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bwi Inc.
FDA (openFDA food enforcement)
Reported Feb 22, 2017
LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral hip stem is made up of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific 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.