All recall categories

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.

Medical devices

Reported Mar 4, 2015

The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…

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)

Food

Reported Mar 4, 2015

Chili-Bean Fresh Veggiburger, 4 Pre-Grilled Patties, All Natural Meatless Patties, Net Wt. 10 oz. (284)g)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

J P Veggies Inc. dba VeggieLand

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2015

Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2015

The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2015

La Flor ground COMINO, 1) NET WT. 2 OZ, 2) NET WT 6 OZ (170.1g), 3) NET WT. 5 LBS. Packed By La Flor Products Co.,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

La Flor Products Co., Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Feb 10, 2015

Whole Foods Markets, Inc. Retira Productos Debido A Un Posible Error De Rotulacin Y A Un Alrgeno No Declarado

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Recalling firm not stated

USDA FSIS

Medical devices

Reported Jan 28, 2015

Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2015

PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Genetic Testing Institute,Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2015

iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brainlab AG

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 21, 2015

Harvest Blend, Net Wt. 4 oz. (113g) Best If Enjoyed By: 12/05/2014, DISTRIBUTED BY 7-ELEVEN, INC., DALLAS, TX 75201 UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Del Monte Fresh Produce NA, Inc.

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 21, 2015

The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized in knee replacement procedures. The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2015

Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447S Endosseous dental implant…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Straumann USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2015

Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Centurion Medical Products Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2015

CSA Medical truFreeze System; Model: CC3-01, a cryogenic surgical device ***The involved units are those with the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CSA Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2015

Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION Impactors are re-useable instruments utilized in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Orthopaedics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2015

Cable remote control JUPITER U, Material no.4500119, Serial number: to (incl.) 102306915. Patient positioning during…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Trumpf Medical Systems, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 14, 2015

Vintage Pure Bee Flower Honey, Net Weight 16.4 oz (465g), Packaged in a Glass Jar, Product of Turkey, Imported by:…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Vintage Food Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 7, 2015

Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

ADULT Radiotransparent Electrode, Part number C100-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Heart Sync, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2014

RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mako Surgical Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2014

Oceans Catch All Natural Jonah Crab Combo Meat, Packaged in round plastic containers (tub with snap-on lid), sold…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Rome Packing Co., Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2014

Amerigel Hydrogel Wound Dressing Wound management

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2014

MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microgenics 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.