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.
Reported May 20, 2026
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 13, 2026
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe Medical, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
XZL, Jelly Snacks, 12.68 OZ, Bag. 12 Bags per Case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sungal Inc.
FDA (openFDA food enforcement)
Reported May 6, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator, 6mm-7mm-8mm, REF 1204-08
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diversatek Healthcare
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2026
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ajinomoto Foods North America Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 1, 2026
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Merit Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Savannah Bee Company Inc.
FDA (openFDA food enforcement)
Reported Mar 25, 2026
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Winder Laboratories, LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2026
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Mar 4, 2026
Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus…
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)
Reported Mar 4, 2026
MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MRIMed Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2026
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2026
EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705
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)
Reported Feb 11, 2026
Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for their…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imu-Tek Animal Health, Incorporated
FDA (openFDA food 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.