State

Rhode Island product recalls

73,088 recalls have nationwide distribution and so reach Rhode Island. 3,046 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,046
Critical: 221
Severe: 572
Most recent: 2026-09-23

Of the 3,046 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 572 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,046 recalls whose distribution notice names Rhode Island specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8826–8850 of 76134

LowFDA (Devices)·Z-0557-2025·2024-12-04
Tempus LS-Manual Defibrillator Recalled for Incorrect Servicing Labels
Remote Diagnostic Technologies Ltd. is recalling Tempus LS-Manual Defibrillator Model 00-3020 units distributed in eight U.S. states. The devices were labeled incorrectly during servicing with wrong product name and CAT number.
Product
Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V908000·2024-12-03
2025 Kenworth T880 steering fasteners may fail and cause crashes
PACCAR is recalling 2025 Kenworth T880 and other commercial vehicles due to steering arm and tie rod bracket fasteners that may fail, resulting in loss of steering control and increased crash risk.
Product
PETERBILT — PETERBILT, KENWORTH 520, T480, 548, 367
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V907000·2024-12-03
Nova Bus recalls 2022-2024 LFS buses for wheelchair restraint defect
Nova Bus recalled 2022-2024 LFS buses for incorrectly installed wheelchair securement systems. The attachment points may be in wrong locations, preventing proper restraint in crashes.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V906000·2024-12-03
International Recalls 2025 EMV Vehicles Due to Missing Defrost Circuit Breaker
International is recalling 2025 EMV vehicles because a missing circuit breaker may cause the windshield defrosting system to fail, reducing visibility.
Product
INTERNATIONAL — INTERNATIONAL EMV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V905000·2024-12-02
Pierce Fire Trucks Recalled for Incompatible Front Tires and Wheels
Pierce is recalling 2023-2024 Velocity, Enforcer, and Quantum fire trucks because front steer axle tires are incompatible with the wheels, increasing crash risk.
Product
PIERCE — PIERCE VELOCITY, ENFORCER, QUANTUM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V904000·2024-12-02
Tesla Recalls 2024 Model X Vehicles Due to Flickering Headlights
Tesla is recalling 2024 Model X vehicles because flickering parking lights and low beam headlights may fail to sufficiently illuminate the roadway, increasing crash risk.
Product
TESLA — TESLA MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-12022024-01·2024-12-02
USDA Issues Public Health Alert for Ineligible Imported Pork Mortadella
USDA FSIS issued a public health alert for frozen pork mortadella illegally imported from Ecuador. Consumers should discard the product as it lacks required inspection marks.
Product
FSIS Issues Public Health Alert for Ineligible Pork Products Imported From Ecuador
Category
Food
Distribution
1 state
HighNHTSA·24V903000·2024-12-02
Kenworth and Peterbilt Trucks Recalled for Insufficient Axle Bearing Lubrication
PACCAR is recalling 2024-2025 Kenworth and Peterbilt commercial trucks with insufficient axle bearing lubrication, which may cause wheel hub overheating and fire or loss of vehicle control.
Product
KENWORTH — KENWORTH, PETERBILT T380, T480, 536, 537
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V902000·2024-11-29
Kuntry Kustom Recalls 2023-2024 Rich Specialty Trailers Due to Fire Risk
Kuntry Kustom RV is recalling 2023-2024 Rich Specialty Sanitation and Office trailers because a faulty air conditioner component may overheat and cause a fire.
Product
RICH SPECIALITY TRAILERS — RICH SPECIALITY TRAILERS OFFICE, SANITATION
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V901000·2024-11-28
McLaren Recalls 2021 765LT Coupe for Rear Window Adhesive Defect
McLaren is recalling 163 2021 765LT Coupe vehicles because the rear cabin window may detach due to insufficient adhesive bonding, creating a road hazard.
Product
MCLAREN — MCLAREN 765LT
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0382-2025·2024-11-27
Baxter Peritoneal Dialysis Transfer Sets Recalled for Chemical Exposure
Baxter Healthcare Corporation is recalling 1,240 units of MiniCap Extended Life PD Transfer Sets (Part Number T5C4484) due to potential exposure to polychlorinated biphenyls and related compounds when used in peritoneal dialysis treatments.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short, Part Number T5C4484; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0378-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set recalled for potential PCB exposure
Baxter Healthcare is recalling 58,680 units of its MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Users should stop using affected units and consult their healthcare provider.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0377-2025·2024-11-27
Baxter Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk
Baxter Healthcare is recalling the MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Approximately 410,862 units are affected.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0482-2025·2024-11-27
Medical Device Recall: Counterfeit Batteries in Plum Infusion Systems
Counterfeit CSB batteries are being used in Plum Infusion Systems. These unauthorized batteries fail to hold their charge and have not been tested for use with the pumps.
Product
Allegedly counterfeit batteries manufactured by CSB batteries being used with Plum Infusion Systems: Plum 360" Infusion System, Pump List Number 30010; Plum A+ & Plum A+3" Infusion Systems, Pump List Numbers: 11005, 11971, 12391, 12618, 20678, 20679, 20792, 60529, 12348, 1197
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0379-2025·2024-11-27
Baxter MiniCap Dialysis Transfer Sets Recalled for PCB Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets used in peritoneal dialysis due to potential exposure to polychlorinated biphenyls (PCBs). About 62,394 units distributed worldwide may be affected.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0373-2025·2024-11-27
Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk
Baxter Healthcare recalls peritoneal dialysis transfer sets (Part Number 5C4482) due to potential contamination with polychlorinated biphenyls (PCBs). The recall affects 2.7 million units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V896000·2024-11-27
Chrysler Recalls 2017-2018 Ram Trucks Due to Brake Control Unit Failure
Chrysler is recalling 2017-2018 Ram 2500, 3500, 4500, and 5500 trucks because the hydraulic control unit may fail, disabling anti-lock brakes and stability controls.
Product
RAM — RAM 5500, 2500, 4500, 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V900000·2024-11-27
Honda Passport and Pilot fuel filler pipes can separate and leak
Honda is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles because the fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Product
HONDA — HONDA PASSPORT, PILOT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0375-2025·2024-11-27
Baxter peritoneal dialysis transfer set recalled for PCB exposure risk
Baxter MiniCap Extended Life PD Transfer Sets (Part 5C4482S) are being recalled due to potential exposure to polychlorinated biphenyls (PCBs). The FDA Class I recall affects 151,020 units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V897000·2024-11-27
Jeep Grand Cherokee side airbags may not deploy in a crash
Chrysler is recalling certain 2022-2024 Grand Cherokee and 2021-2024 Grand Cherokee L vehicles because an improperly secured connector may prevent the front seat side airbags deploying. All units have been remedied.
Product
JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V899000·2024-11-27
Keystone Recalls 2025 Arcadia and Cougar Trailers for Hitch Fastener Issue
Keystone is recalling 2025 Arcadia and Cougar trailers because improperly tightened pin box fasteners may loosen, allowing the trailer to detach and increasing crash risk.
Product
KEYSTONE — KEYSTONE COUGAR, ARCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V898000·2024-11-27
Audi plug-in hybrid high voltage batteries can overheat
Volkswagen is recalling certain 2022-2023 Audi Q5 PHEV and 2022 Audi A7 PHEV vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24C002000·2024-11-27
Nuna Rava Child Seat Recall for Harness Adjuster Defect
Nuna is recalling Rava child seats where debris may cause the harness adjuster to fail, potentially leaving the harness loose in a crash.
Product
CHILD SEAT:HARNESS:FRONT ADJUSTER BUTTON/RELEASE MECHANISM recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0484-2025·2024-11-27
Maquet Cardiovascular Recalls Acrobat-i Positioners Due to Sterility Concerns
Maquet Cardiovascular is recalling 14,338 Acrobat-i Positioners because manufacturing deviations compromised the sterile barrier, meaning sterility cannot be assured during the product's 2-year shelf life.
Product
Acrobat-i Positioner. Model Number C-XP-5000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0052-2025·2024-11-27
FDA recalls Ramipril 2.5 mg capsules for manufacturing control deviations
Lupin Pharmaceuticals is recalling Ramipril 2.5 mg capsules after sourcing the active ingredient from an unapproved vendor. Approximately 112,770 bottles were distributed to wholesalers nationwide.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide