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 Nov 16, 2022
Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iRhythm Technologies, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Sedecal Soltus Battery Mobile X-Ray System REF Soltus 450 Battery Mobile X-Ray System REF Soltus 500
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal Sa
FDA (openFDA device enforcement)
Reported Nov 9, 2022
BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2022
BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2022
Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bella Brands, LLC dba Bella Cucina Artful Food
13 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2022
EKOS Control Unit 4.0 console, a component of the EKOS Control System 4.0, which is a component of the EkoSonic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2022
Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2022
Food Club Chive Cottage Cheese, 16 oz; Hannaford Chive Cottage Cheese, 16 oz; Hood Chive Cottage Cheese, 16 oz and 24…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HP Hood LLC
12 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 2, 2022
CorVocet Biopsy System/Catalog Code: CORA1610/B, CORA1610S/B, CORA1615/B, CORA1810/A, CORA1810/B, CORA1810S/B,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 2, 2022
THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Chai Box
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 2, 2022
AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Circulation, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2022
Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2022
Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods (Corporate Offices)
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2022
Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lyons Magnus LLC
11 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2022
Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seeking Health LLC
FDA (openFDA food enforcement)
Reported Oct 12, 2022
Philips Respironics Amara View Minimal Contact Full-Face Mask
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DICOM Grid, Inc. d/b/a Ambra Health
FDA (openFDA device enforcement)
Reported Oct 5, 2022
MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 21, 2022
MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 21, 2022
Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Various Angiography packs/trays
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
16 more products in this recall
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.