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.

Food

Reported Jan 3, 2024

Bowl & Basket Zero Calorie with Sucralose Sweetener 100 count, UPC 0-41190-06855-5, 12 retail cartons per wholesale case

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

Wakefern Foods Corp.

FDA (openFDA food enforcement)

Food

Reported Dec 27, 2023

Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356,…

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

Kenover Marketing Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

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

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 20, 2023

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

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

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

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

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2023

CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.

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

Stanbio Laboratory, LP

FDA (openFDA device enforcement)

Food

Reported Dec 13, 2023

Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 084648311285

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 6, 2023

BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

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

Becton Dickinson Infusion Therapy Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…

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

Beckman Coulter Biomedical Division

FDA (openFDA device enforcement)

Meat & poultry

Reported Nov 19, 2023

Skyline Provisions, Inc. Recalls Raw Ground Beef Products Due to Possible Foreign Matter Contamination

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

Skyline Provisions

USDA FSIS

Medical devices

Reported Nov 15, 2023

BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.

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

Breg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

DJO EMPOWR Knee Punch Handle, REF: 801-05-040

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

Encore Medical, LP

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Frozen and fresh RTE Lobster meat (1 lb. packages to 12 lb. case) 1. Greenhead Lobster HPP Fresh Cooked Claw and…

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

Greenhead Lobster Products LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Nutricia KetcoCal 4:1 LQ Unflavored in 237ml (8fl oz) packaged in tetra prisma paper aseptic carton - 3 cartons per box…

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

Nutricia North America

FDA (openFDA food enforcement)

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Other states

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.