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 Mar 13, 2013
Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For temporary (<30 days) use with recording,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Deep Best Quality Dry Garlic Chutney (Thechaa); Net Wt. 4 OZ.; UPC 011433111201; Deep Foods, Inc. Union, NJ 07083
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deep Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 13, 2013
PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Synthes Multi-Vector Distractor Body, Part Number 487.931. For mandibular bone lengthening.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Organic Lemon Grass Tea Bag Cut (TBC), Item#410. Packing Size: 25 kgs net double craft paper bags and double…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Qtrade Teas And Herb
FDA (openFDA food enforcement)
Reported Mar 6, 2013
Whole Foods Market Whole Catch Wild Alaskan Sockeye Smoked Salmon, Cold Smoked Sliced, Net Wt. 4 oz, Distributed by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 27, 2013
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Animas Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2013
LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2013
St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Jude Medical Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
SeriScaffold Surgical Scaffold Product Number: SCF10X25AGEN. Surgical mesh for use in open or laparoscopic procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergen Medical
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diagnostic Hybrids Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
THERA PEARL 3-in-1 BREAST THERAPY, 2 hot and cold packs in plastic box. The Thera Pearl 3-in-1 Breast Therapy is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lansinoh Laboratories Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Oxoid Antimicrobial Susceptibility Test Discs, Aztreonam 30 ug, IVD, REF CT0264B, Oxoid Ltd., UK, oxoid@thrmofisher.com…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2013
BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Esteem Programmer Model 6001, US and ISA, Model 3001 Dell E54XX, part of the Esteem Totally Implantable Hearing System.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Envoy Medical Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Jan 30, 2013
Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Cold-smoked salmon in vacuum plastic bags that are partially clear and partially colored black, white, gold and pink.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ocean Beauty Seafoods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 23, 2013
Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Woodstock Farms
FDA (openFDA food enforcement)
Reported Jan 2, 2013
Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Curve catalog no.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greatbatch Medical
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.