State

Rhode Island product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37801–37825 of 76794

ModerateFDA (Devices)·Z-0239-2019·2018-10-31
Philips DigitalDiagnost Software Recall for X-ray System Stitching Defects
Philips is recalling DigitalDiagnost software for stationary X-ray systems due to intermittent stitching interruptions and incorrect baseline data on the system CD.
Product
Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0092-2019·2018-10-31
Lupin Recalls Fluocinolone Acetonide Topical Solution Due to Impurity Failures
Lupin Pharmaceuticals is recalling 2,712 bottles of Fluocinolone Acetonide Topical Solution because stability testing showed total impurities exceeded specifications.
Product
FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0218-2019·2018-10-31
BioMerieux NucliSENS Magnetic Extraction Reagents Recalled Due to Temperature Exposure
BioMerieux is recalling 42 units of NucliSENS Magnetic Extraction Reagents because data loggers indicated one shipment experienced low temperatures that may impact performance.
Product
NucliSENS¿ Magnetic Extraction Reagents
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0233-2019·2018-10-31
Ecolab Recalls Disposable Accessory Kits for Da Vinci Robotic System
Ecolab Inc is recalling specific lots of Disposable Accessory Kits, 3-Arm, due to potential pouch seal defects that could compromise sterility.
Product
Disposable Accessory Kit, 3-Arm (Box of 5) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0281-2019·2018-10-31
Upsher Smith Recalls Bumetanide Tablets for Unspecified Degradation Product
Upsher Smith Laboratories is recalling 29,080 bottles of Bumetanide 2 mg tablets because the product failed impurity specifications for an unspecified degradation product.
Product
BUMETANIDE — BUMETANIDE (BUMETANIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0230-2019·2018-10-31
bioMerieux Recalls BACT/ALERT VIRTUO Systems Due to Firmware Calibration Issue
bioMerieux is recalling 8 BACT/ALERT VIRTUO systems because firmware version R2.0 allows calibration standards to be moved, potentially causing anomalies if not returned to designated locations.
Product
BACT/ALERT VIRTUO system, A Unit China, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection System is an automated microbial test system capable of incubating, agitating, and continuously monitoring for the detection of aerobic, facultative…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0237-2019·2018-10-31
Micro-Tech Recalls Single-Use Biopsy Forceps Due to Incorrect Product Contents
Micro-Tech (Nanjing) Co., Ltd. is recalling 1,360 units of Single-Use Biopsy Forceps because the boxes contained Grasping Forceps instead of the labeled product.
Product
Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0089-2019·2018-10-31
Westlab Pharmacy Recalls Alprostadil Injectable Vials Due to Incorrect Formulation
Westlab Pharmacy is recalling 80 vials of Alprostadil 500 mcg/mL Injectable due to an incorrect product formulation. The recall covers nationwide distribution.
Product
Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·19026·2018-10-31
Fantasia Accessories Recalls Slap Bracelets Due to Laceration Hazard
Fantasia Accessories is recalling about 22,500 children's slap bracelets sold at Target because the metal band can pierce the fabric cover, posing a laceration hazard.
Product
Slap bracelets
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0130-2019·2018-10-31
RXQ Compounding Recalls Subpotent Lidocaine and Epinephrine Injection Vials
RXQ Compounding LLC is recalling 395 vials of Lidocaine 1% + Epinephrine 1:100,000 injection solution because testing revealed the product was subpotent.
Product
Lidocaine 1% + Epinephrine 1:100,000 (MDV) INJ SOL, 50 mL per glass vial, Rx only, 340 West State Street, Unit 9, Athens, OH 45701. NDC 7073197450
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0235-2019·2018-10-31
Stryker Altrix Temperature Management System Recalled for Alarm Faults
Stryker is recalling 389 Altrix Precision Temperature Management Systems due to frequent alarms and mechanical interference faults.
Product
Altrix¿ Precision Temperature Management System Model: 8001Product Usage: The Altrix system is intended for circulating temperature controlled warm or cold water via patient contact thermal transfer devices for the application of regulating human body temperature in situations…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0229-2019·2018-10-31
bioMerieux Recalls BACT/ALERT VIRTUO Systems Due to Firmware Calibration Issue
bioMerieux is recalling 151 BACT/ALERT VIRTUO systems with R2.0 firmware because a software feature may allow calibration standards to be left in incorrect positions, potentially causing anomalies.
Product
BACT/ALERT VIRTUO system, B Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection System is an automated microbial test system capable of incubating, agitating, and continuously monitoring for the detection of aerobic, facultative, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0227-2019·2018-10-31
Terumo Recalls VirtuoSaph Plus Endoscopic Vessel Harvesting System
Terumo is recalling 135 units of the VirtuoSaph Plus Endoscopic Vessel Harvesting System because one energy platform is not compatible with the device.
Product
VirtuoSaph Plus Endoscopic Vessel Harvesting System, Catalog Number: VSP550EX Product Usage: The VittuoSaph¿ Plus Endoscopic Vessel Harvesting System VSP550EX is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily indicated…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0228-2019·2018-10-31
bioMerieux Recalls BACT/ALERT VIRTUO Systems Due to Firmware Calibration Issue
bioMerieux is recalling 516 BACT/ALERT VIRTUO systems with R2.0 firmware because a service feature may leave calibration standards in incorrect locations, potentially causing anomalies.
Product
BACT/ALERT VIRTUO system, A Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection System is an automated microbial test system capable of incubating, agitating, and continuously monitoring for the detection of aerobic, facultative, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0231-2019·2018-10-31
Ecolab recalls sterile instrument arm drapes due to potential seal defects
Ecolab is recalling specific lots of sterile instrument arm drapes for the Da Vinci Si system because seal wrinkles may compromise sterility.
Product
Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system Distribute by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to cover/wrap…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0087-2019·2018-10-31
Lupin Recalls Testosterone Topical Solution Due to Defective Pump
Lupin Pharmaceuticals is recalling 6,752 bottles of Testosterone Topical Solution because the pump mechanism is not working.
Product
TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0239-2019·2018-10-31
Promise Pharmacy Recalls Prednisolone and Gatifloxacin Ophthalmic Solution Due to Precipitate
Promise Pharmacy LLC is recalling Prednisolone and Gatifloxacin Ophthalmic Solution due to the presence of precipitate. The recall covers nationwide distribution.
Product
Prednisolone and Gatifloxacin Ophthalmic Solution, 1%/0.5%, 3 mL dropper bottle, Rx Only, 31818 US Hwy 19N, Palm Harbor, FL 34684
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V762000·2018-10-30
Altec Recalls 2009 Aerial Devices Due to Riser Assembly Cracking Risk
Altec Industries is recalling 2009 LSS 60 and LSS 70 Elevator Aerial devices because the elevator riser assembly may crack and fail, increasing the risk of injury or death.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E098000·2018-10-30
Hickory Springs Recalls School Bus Seats Due to Pedestal Bolt Fracture Risk
Hickory Springs is recalling specific school bus seats because bolts securing the seat pedestal to the floor may fracture, potentially increasing injury risk during a crash.
Product
SEATS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V763000·2018-10-30
Thor Motor Coach Recalls 2017-2019 Models for Lighting Defect
Thor Motor Coach is recalling 1,769 motorhomes because a damaged power distribution module may cause rear lights or turn signals to fail, increasing crash risk.
Product
THOR — THOR, THOR MOTOR COACH ARIA, PALAZZO, TUSCANY, VENETIAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V766000·2018-10-30
Volvo Recalls VHD Trucks for Snow Plow Lighting Defect
Volvo is recalling 2004-2019 VHD trucks with snow plow kits because the headlights can operate without other exterior lights, reducing visibility.
Product
VOLVO — VOLVO VHD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V764000·2018-10-30
Grand Design Recalls 2018-2019 Reflection Trailers Due to Fire Risk
Grand Design RV is recalling 2018-2019 Reflection fifth wheel trailers because the power converter circuit lacks over-current protection, increasing the risk of fire.
Product
GRAND DESIGN — GRAND DESIGN REFLECTION
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V765000·2018-10-30
Mack Recalls 2019 Granite Trucks Due to Snow Plow Lighting Defect
Mack is recalling 2019 Granite trucks with snow plow kits because the headlights can operate without other exterior lights, reducing visibility.
Product
MACK — MACK GRANITE (GU)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V759000·2018-10-29
2018 Jeep Grand Cherokee SRT and Trackhawk Floor Mat Recall
Chrysler is recalling 2018 Jeep Grand Cherokee SRT and Trackhawk vehicles because the driver's floor mat may prevent the accelerator pedal from returning to idle, increasing crash risk.
Product
JEEP — JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18E097000·2018-10-29
Chrysler Recalls Mopar Floor Mats for 2018 Jeep Grand Cherokee SRT
Chrysler is recalling specific Mopar floor mats for 2018 Jeep Grand Cherokee SRT and Trackhawk models because they may interfere with the accelerator pedal, increasing crash risk.
Product
JEEP — JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide