State

Rhode Island product recalls

73,738 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,053
Critical: 221
Severe: 707
Most recent: 2026-10-28

Of the 3,053 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34326–34350 of 76791

LowFDA (Drugs)·D-1490-2019·2019-07-24
Lupin Recalls Gatifloxacin Ophthalmic Solution Due to Missing Labels
Lupin Pharmaceuticals is recalling 17,238 bottles of Gatifloxacin Ophthalmic Solution 0.5% because some bottles were found missing their labels.
Product
Gatifloxacin Ophthalmic Solution 0.5%, For Use in the Eyes Only, Rx Only, Sterile, 2.5 mL Bottle, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India, NDC 68180-435-01.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1974-2019·2019-07-24
Teleflex Medical Recalls RUSCH CARE Premium Drain Bags for Labeling Issues
Teleflex Medical is recalling RUSCH CARE Premium Drain bags because the labels are not UDI compliant. The agency states this labeling issue is not likely to affect the device's function or performance.
Product
RUSCH CARE Premium Drain bag, 2000mlm REF 390000 urine collection device
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1975-2019·2019-07-24
Teleflex Medical Recalls RUSCH Urinary Drainage Bags for Labeling Issues
Teleflex Medical is recalling RUSCH Urinary Drainage bags because the labels are not UDI compliant. The missing information does not affect the device's function or performance.
Product
RUSCH Urinary Drainage bag, 2000mlm REF 390060 urine collection device
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V541000·2019-07-23
BMW Recalls 2019 X5 and X7 Models for Loose Wheel Bolts
BMW is recalling 2019 X5 xDrive50i and X7 xDrive40i vehicles because left-side wheel bolts may loosen, increasing the risk of a crash.
Product
BMW — BMW X7, X5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19E048000·2019-07-23
Darsan Trading Recalls HCI 100 Motorcycle Helmets for Safety Standard Failures
Darsan Trading Co. is recalling HCI 100 matt black motorcycle helmets in size XL because they may not adequately protect the wearer in a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·19171·2019-07-23
Boppy Infant Head and Neck Support Accessories Recalled for Suffocation Hazard
The Boppy Company is recalling infant head and neck support accessories because the overstuffed design can tilt an infant's head forward, posing a suffocation risk.
Product
Boppy Infant Head and Neck Support Accessories
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19E046000·2019-07-19
MORryde Recalls Fifth Wheel Wedge Kits Due to Incorrect Bolts
MORryde is recalling certain Orbital and You Turn Rubber Pin Box Wedge Kits because incorrect bolt lengths may prevent proper tightening, increasing crash risk.
Product
TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19E047000·2019-07-19
MORryde Recalls Fifth Wheel Pin Boxes Due to Short Bolts
MORryde is recalling certain You Turn and Orbital Rotating Pin boxes because they may have shorter bolts than required, increasing the risk of a crash.
Product
TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V538000·2019-07-19
Hyundai Recalls Genesis G80 and G90 Vehicles for Oil Leak Fire Risk
Hyundai is recalling 2018 Genesis G80 and 2017-2018 Genesis G90 vehicles because a loose seal may cause oil to leak onto the exhaust manifold, increasing fire risk.
Product
GENESIS — GENESIS G90, G80
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V539000·2019-07-19
Kia Recalls 2019 Optima Vehicles for Forward Collision Avoidance Software Error
Kia is recalling 2019 Optima vehicles because a software error may prevent the automatic emergency braking system from engaging when a stationary vehicle is detected.
Product
KIA — KIA OPTIMA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V540000·2019-07-19
Mercedes-Benz Recalls Vehicles for Radar Sensor Software Error
Mercedes-Benz is recalling 2019-2020 vehicles because a software error in the radar sensor may impair Active Brake Assist, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ CLS 450, C 300, E 450, E 300
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19170·2019-07-18
Factory Direct Wholesale Recalls Folding Mattresses for Flammability Violation
Factory Direct Wholesale is recalling about 2,500 folding mattresses because they fail to meet the federal flammability standard, posing a fire hazard.
Product
Folding mattresses
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1465-2019·2019-07-17
Losartan Potassium Tablets Recalled Due to NMBA Impurity Detection
Golden State Medical Supply Inc. is recalling Losartan Potassium 100 mg tablets because an impurity called NMBA was detected in the active ingredient.
Product
Losartan Potassium, 100 mg tablets, 90 count bottle, NDC 60429-318-90
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1459-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1770-2019·2019-07-17
Becton Dickinson Recalls Alaris Pump Infusion Sets Due to Occlusion Defect
Becton Dickinson is recalling Alaris Pump Infusion Sets because a wall thickness variation can cause incomplete occlusion, potentially leading to unintended or faster-than-expected medication delivery.
Product
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930, 11522558, 11607704, 10013361T, 2110-0500, 2126-0500, 2200-0500, 2411-0500, 2419-0007, 2420-0007, 2420-0500, 2421-0500, 2426-0007, 2426-0500, 2429-0500…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1847-2019·2019-07-17
GE Healthcare Recalls Panda Infant Radiant Warmers Due to Bedside Panel Cracking
GE Healthcare is recalling 28,094 Panda Infant Radiant Warmers because the bedside panels and latch areas can crack or break if the unit is moved using them instead of the designated handles.
Product
Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition to the external environment…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19E045000·2019-07-17
Reyco Fire Truck Front Suspension Recall for Shock Separation Risk
Reyco is recalling Fire Truck Independent Front Suspensions because front shocks may separate and damage the steering gear, potentially causing a loss of power steering assist.
Product
SUSPENSION:FRONT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1455-2019·2019-07-17
Teva Recalls Losartan Potassium Tablets Due to Impurity Detection
Teva Pharmaceuticals USA is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles, NDC 00591-3746-00
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1460-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active pharmaceutical ingredient.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1466-2019·2019-07-17
Major Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity
Major Pharmaceuticals is recalling Losartan Potassium 50 mg tablets because FDA testing found an impurity above acceptable levels.
Product
Losartan Potassium Tablets, USP. 50 mg. NDC# 0904-6390-61. Rx only. 100 count Unit Dose Cartons. Manufactured by Major Pharmaceuticals 17177 N. Laurel Park Drive Suite 233, Livonia, MI 48152.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1461-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1923-2019·2019-07-17
Philips HeartStart MRx Recall Due to AC Power Module Failure Risk
Philips is recalling HeartStart MRx devices used with specific AC power modules that may fail, potentially causing loss of power and failure to deliver shocks.
Product
Philips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1874-2019·2019-07-17
Hamilton Medical Recalls HAMILTON-G5 Ventilators Due to Ambient State Risk
Hamilton Medical is recalling 4,338 HAMILTON-G5 ventilators with software versions 2.60 or lower because they may enter an ambient state, requiring immediate alternative ventilation.
Product
HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for intensive care ventilation of adult and pediatric patients, and optionally infant and neonatal patients. The device is intended for use in the hospital and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1462-2019·2019-07-17
Losartan Potassium Tablets Recalled Due to Impurity Detection
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Product
Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1464-2019·2019-07-17
Losartan Potassium Tablets Recalled Due to Nitrosamine Impurity
Golden State Medical Supply is recalling Losartan Potassium 50 mg tablets because a nitrosamine impurity was detected in the active ingredient.
Product
Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10
Category
Drug
Distribution
Distributed nationwide