The Recall Desk

State

Rhode Island product recalls

73,817 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

Of the 3,054 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 708 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49326–49350 of 76871

  • ModerateFDA (Devices)·Z-2275-2016·2016-08-03

    Pentax Medical Video Processor Recalled for Uncleared Water Bottle Assembly

    Pentax Medical is recalling the EPK-i5010 Video Processor because it was shipped with a water bottle assembly not cleared for use in the United States.

    Product
    Colonoscope Product Usage: Intended to provide optical visualization of and therapeutic access to the Lower Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: Large Bowel to the Cecum. The instrument is introduced…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2276-2016·2016-08-03

    Pentax Medical Video Processor Recalled for Uncleared Water Bottle Assembly

    Pentax Medical is recalling Video Processor EPK-i5010 units shipped with a water bottle assembly not cleared for US use.

    Product
    Confocal GI Scope Product Usage: Intended to provide optical visualization of and therapeutic access to the Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: Esophagus, Stomach, Duodenum, and Large Bowel to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2277-2016·2016-08-03

    Pentax Medical Video Processor Recalled for Uncleared Water Bottle Assembly

    Pentax Medical is recalling the EPK-i5010 Video Processor because it was shipped with a water bottle assembly not cleared for use in the United States.

    Product
    Duodenoscope Product Usage: Intended to provide optical visualization of and therapeutic access to the Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: Esophagus, Stomach, Duodenum, and Large Bowel to the Cecum.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2288-2016·2016-08-03

    LeMaitre Vascular Recalls Anastoclip Universal Clip Remover for Mislabeling

    LeMaitre Vascular is recalling 55 units of the Anastoclip Universal Clip Remover because marketing materials incorrectly stated the device could be used for dura closure.

    Product
    AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip Clip applier consists of a rotating shaft and an integral cartridge containing titanium clips. The Anastoclip Universal Clip Remover is intended to remove Anastoclip AC Clips as necessary. It is an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2286-2016·2016-08-03

    LeMaitre Vascular Recalls Anastoclip Universal Clip Remover for Mislabeling

    LeMaitre Vascular is recalling the Anastoclip Universal Clip Remover because marketing materials incorrectly stated the device could be used for dura closure, though it is only intended for cardiovascular use.

    Product
    AnastoCiip Universal Clip Remover (6 Pack} REF# 4001-00 The Anastoclip Clip applier consists of a rotating shaft and an integral cartridge containing titanium clips. The Anastoclip Universal Clip Remover is intended to remove Anastoclip AC Clips as necessary. It is an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2285-2016·2016-08-03

    LeMaitre Vascular Recalls Anasto AC Closure System for Mislabeling

    LeMaitre Vascular is recalling 170 units of the Anasto AC Closure System because marketing materials incorrectly stated the device could be used for dura closure.

    Product
    Anasto AC Closure System and Anasto Universal Clip Remover- Anasto AC 8cm 25 Clips (1 Each} X-Large REF # 4000-08 The Anastoclip Clip applier consists of a rotating shaft and an integral cartridge containing titanium clips. The Anastoclip Universal Clip Remover is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1451-2016·2016-08-03

    Teva Recalls MitoXANTRONE Injection Due to High Impurity Levels

    Teva North America is recalling 2,506 vials of MitoXANTRONE Injection USP because high levels of Impurity D were detected.

    Product
    mitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial packaged in a carton, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-4685-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2282-2016·2016-08-03

    Tosoh Bioscience Recalls Progesterone 3 Calibrator Sets Due to Incorrect IFU Lot Number

    Tosoh Bioscience is recalling 41 sets of Progesterone 3 Calibrators because the included Instructions for Use (IFU) listed the incorrect lot number.

    Product
    Instructions for Use (IFU) for Progesterone 3 Calibrator Set, repackaged as one set/package. The Instructions for Use (IFU) included in the package was for the incorrect lot number. Only the IFU required correction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V572000·2016-08-02

    Aluma/KLM Recalls 2011-2015 Trailers Due to Missing Welds

    Aluma/KLM is recalling 2011-2015 5410T and 5410WD trailers because missing welds may cause the tongue to separate, increasing crash risk.

    Product
    ALUMA KLM — ALUMA KLM 5410T, 5410WD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16236·2016-08-02

    Starbucks Recalls Stainless Steel Straws Due to Mouth Laceration Risk

    Starbucks is recalling approximately 2.5 million stainless steel straws sold in the U.S. because the rigid design poses a risk of mouth lacerations to young children.

    Product
    Stainless Steel Straws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V574000·2016-08-02

    Hyundai Recalls 2013 Elantra Vehicles for Brake Pedal Stopper Pad Defect

    Hyundai is recalling 64,500 2013 Elantra vehicles because a deteriorating brake pedal stopper pad can prevent the brake light switch from retracting, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16237·2016-08-02

    BYA Sports Recalls Double Hammocks Due to Fall Hazard

    BYA Sports is recalling approximately 760 double hammocks because a weld on the metal ring can fail, causing the hammock to fall and posing a fall hazard to users.

    Product
    Bring Your Adventure (BYA) Sports hammocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V571000·2016-08-02

    Thor Motor Coach Recalls Motorhomes Due to Flammable Shower Curtains

    Thor Motor Coach is recalling specific 2012-2017 motorhomes because the shower curtains may not resist catching fire, increasing injury risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, ROAD BEAR RENTAL, CITATION, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V566000·2016-08-01

    Heartland Recalls Travel Trailers Due to Fire Risk from LED Light

    Heartland is recalling specific 2015-2017 travel trailers and fifth wheels because an LED light may short circuit and overheat, increasing fire risk.

    Product
    HEARTLAND — HEARTLAND MALLARD, ELKRIDGE, SUNDANCE, WILDERNESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·059-2016 EXP·2016-08-01

    Michael Angelo's Recalls Frozen Shrimp Scampi and Meat Lasagna for Allergens

    Michael Angelo's Gourmet Foods is recalling 5,677 pounds of frozen shrimp scampi and meat lasagna due to misbranding and undeclared allergens like chicken, egg, soy, and shrimp.

    Product
    Michael Angelo's Gourmet Foods Inc. — Michael Angelo's Gourmet Foods, Inc. Recalls Shrimp Scampi and Meat Lasagna Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V569000·2016-08-01

    KME Fire Trucks Recalled for Transmission Power Switching Defect

    KME is recalling 112 fire trucks because a transmission component may fail, preventing operators from switching power output needed for firefighting.

    Product
    KME — KME PREDATOR SS, PREDATOR, PREDATOR PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V567000·2016-08-01

    E-One Recalls 2015-2016 Cyclone II and Typhoon Fire Trucks

    E-One is recalling 2015-2016 Cyclone II and Typhoon fire trucks because a transmission component may fail, preventing the vehicle from pumping water to fight fires.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V564000·2016-07-29

    Keystone Recalls 2017 Dutchmen Voltage Trailers Due to Hitch Defect

    Keystone is recalling 2017 Dutchmen Voltage toy haulers because they were built with an incorrect hitch rating. This defect could cause the trailer to separate from the tow vehicle.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V565000·2016-07-29

    Cruiser RV Recalls 2017 Trailers Due to Front Cap Light Fire Risk

    Cruiser RV is recalling 649 model year 2017 recreational trailers because an LED light on the front cap may short circuit and overheat, increasing the risk of fire.

    Product
    CRUISER RV — CRUISER RV SHADOW CRUISER, RADIANCE, MPG, STRYKER TOY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·067-2016·2016-07-28

    Casa Di Trevi Recalls Meat Pasta Products for Undeclared Allergens and Misbranding

    Casa Di Trevi is recalling approximately 845 pounds of meat pasta products that were produced without federal inspection, misbranded, and contain undeclared allergens.

    Product
    DAIRY MAID RAVIOLI MFG. CORP. — Casa Di Trevi Recalls Meat Pasta Products Produced Without Benefit Of Inspection And Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·16234·2016-07-28

    Lekker Recalls Patriot Power Generators Due to Fire Hazard

    Lekker LLC is recalling Patriot Power 1500-watt generators because the battery can catch fire. Consumers should stop using the units and contact 4Patriots for a free replacement.

    Product
    Patriot Power 1500-watt Generator
    Category
    Consumer Product
    Distribution
    Distributed nationwide