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 25, 2020

IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…

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)

Medical devices

Reported Mar 18, 2020

Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555…

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

Medicrea International

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2020

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733

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

Beckman Coulter Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

DeRoyal Sterile Custom Kits containing Cardinal Health Gowns. Sold as the following: Outpatient Major 89-3865.12;

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

Deroyal Industries, Inc. Lafollette

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009

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

Seca

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked Hokkien Noodles - Sweet & Tangy sauce with Bok choy and…

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

CJ Foods Inc., A Division

FDA (openFDA food enforcement)

Food

Reported Mar 4, 2020

Paleonola Grain Free Granola; The Original; packaged in 10oz stand-up pouches; UPC 013964497144

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

Paleonola LLC

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2020

SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…

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

Ormco/Sybronendo

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B

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

Arrow International Inc.

48 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…

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

Market America Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…

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

Medtronic Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…

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

Pacific Medical Group Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon Vinaigrette; Baby Spinach, Hard Boiled Eggs, Monterey…

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

Ready Pac Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213

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

Implant Direct Sybron Manufacturing LLC

FDA (openFDA device enforcement)

Drugs

Reported Feb 12, 2020

Ranitidine Hydrochloride (powder), USP, Rx only, Spectrum Chemical Mfg Corp., a) 1 gram, b) 5 grams, c) 25 grams, d)100…

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

Spectrum Laboratory Products

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…

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

Haemonetics Corporation

21 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Organic IntegriPure Cold Milled Flaxseed, 50 lb Net Wt. and 2000 lb. totes

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

Healthy Food Ingredients, LLC

FDA (openFDA food enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Frozen Yellowfin Tuna, Product of Vietnam, Packaged under the following brands and cuts: Tidal Seafood Tuna Round…

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

Truong Phu Xanh Co.,

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2020

ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…

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

CooperSurgical, Inc.

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.