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 6, 2024

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…

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

Medtronic Neurosurgery

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2024

MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071

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

Mutti USA Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2024

Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129

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

Ready Pac Foods Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2024

Cotija cheese packaged in the following configurations: 1. Sargento Course Grated Cotija Cheese Pack Size 6/5 lb.…

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

Sargento Foods, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 28, 2024

Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.

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

The Procter & Gamble Company

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 7, 2024

MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";

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

Aesculap Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

Rizo Bros Cotija (Grated) 8 oz. UPC 72724200043 7 oz. UPC 7-27242-14022-5 Tio Francisco, Casa Cardenas 9 oz. UPC…

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

Rizo Lopez Foods, Inc. dba Don Francisco Cheese

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66.

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

B-K Medical A/S

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Vermont Village Unsweetened Apple Sauce (24oz)

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Food

Reported Jan 24, 2024

Ministry of Snacks Sweet and Savory Collection #8700

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

Houdini Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 24, 2024

Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871

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

Philips North America

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer…

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

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 17, 2024

Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7

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

Garden Spot Foods, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

Incisive CT, model 728143 & 728144 running Software Version 5.0.0.

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

Philips Healthcare (Suzhou) Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only

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

Natus Medical Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…

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

Philips Respironics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Alinity ci-series System Control Module, REF: 03R70-01

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

Abbott Laboratories

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.