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 Aug 20, 2025

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray…

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

Carefree Surgical Specialties

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2025

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 20, 2025

Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069,…

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Aug 13, 2025

BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 13, 2025

Favorite Day Bakery Frosted Sugar Cookies, 10 count, Net Wt 13.5 oz (383g). UPC - 85239-41250 3. Dist. By Target…

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

Give and Go Prepared Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2025

HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700,…

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

Volcano Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and…

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…

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

Covidien

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2025

Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…

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

Mondelez Global LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2025

Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog…

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

Alcon Research LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. Used in flow cytometry for fluorescence…

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

Becton, Dickinson and Company, BD Bio Sciences

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…

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

Peak Cocktails

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2025

REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number:…

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

Encore Medical, LP

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 2, 2025

FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT. 8 OZ (227g) INGREDIENTS: ORGANIC WHEAT FLOUR, ORGANIC HONEY,…

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

Firehook

FDA (openFDA food enforcement)

Food

Reported Jul 2, 2025

MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies Gluten-Free, Dairy-Free, Allergen Friendly, Egg-Free, Non-GMO, Kosher,…

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

Mightylicious Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 25, 2025

Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in…

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

Preat Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

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

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…

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

Covidien

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.