The Recall Desk

State

Rhode Island product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55076–55100 of 76881

  • LowFDA (Devices)·Z-2066-2015·2015-07-22

    Tosoh Glycohemoglobin Analyzer Buffer Recalled for Incorrect Expiration Date Labeling

    Tosoh Bioscience is recalling G7 Variant Elution Buffer HiS no. 1 (M) because it is labeled with an expiration date of October 2015 instead of the correct October 2014.

    Product
    G7 Variant Elution Buffer HiS no. 1 (M) component of the Tosoh Automated Glycohemoglobin Analyzer HLC 723G7. Product Usage: G7 Variant Elution Buffer HiS No 1. (M) is one of the buffers used on Tosoh Automated Glycohemoglobin Analyzer HLC 723G7.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2090-2015·2015-07-22

    BD Biosciences Recalls Flow Cytometers for Missing Laser Safety Labeling

    BD Biosciences is recalling 2,188 flow cytometers installed between June 2007 and September 2011 because they lack required FDA laser safety labeling.

    Product
    BD Flow Cytometers; used on all BD FACSCount, BD FACSCalibur, BD FACSCanto, BD FACSCanto II, BD LSR II, BD LSRFortessa,BD FACSAria, BD FACSAria II, BD FACSAria Ill, BD lnflux, BD FACSArray,BD Pathway 855, BD Pathway 435 and all SORP instruments. BD Biosciences Flow cytometers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1238-2015·2015-07-22

    Geritrex Recalls Carb-O-Philic 40 Cream Due to Container Closure Deviation

    Geritrex Corp is recalling Carb-O-Philic 40 Cream due to a CGMP deviation involving poor container closure of the bulk storage container.

    Product
    Carb-O-Philic 40 Cream, 40%, a) 3 oz. tube (NDC 54162-640-03) b) 7 oz. tube (NDC 54162-640-07), Rx Only, Manufactured by Geritrex Corporation, Mount Vernon, NY 10550
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1239-2015·2015-07-22

    Qualitest Recalls HydrOXYzine Tablets Due to Unreadable Identification Codes

    Qualitest Pharmaceuticals is recalling HydrOXYzine Hydrochloride 25 mg tablets because some identification codes are unreadable.

    Product
    HydrOXYzine Hydrochloride Tablets, USP 25 mg, Rx only, 100 count (NDC 0603-3968-21), 500 count (NDC 0603-3968-28) and 1000 count (NDC 0603-3968-32) bottles, Manufactured for Qualitest Pharmaceuticals, Huntsville, AL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·15189·2015-07-21

    Acorn Stairlifts Recalls Motorized Stair Lifts Due to Fall Hazard

    Acorn Stairlifts is recalling about 34,500 motorized stair lifts because the seat post can separate from the main support, posing a fall hazard.

    Product
    Motorized stair lifts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V454000·2015-07-21

    Allied Recreation Recalls 2016 Motorhomes Due to Propane Regulator Defect

    Allied Recreation Group is recalling 92 model year 2016 motorhomes because an incorrect propane regulator may allow moisture buildup, potentially causing a gas leak and fire.

    Product
    FLEETWOOD — FLEETWOOD, MONACO, HOLIDAY RAMBLER TIOGA RANGER, TREK, TERRA SE, STORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15188·2015-07-21

    Target Recalls Circo Night Lights Due to Fire Hazard

    Target is recalling about 143,000 Circo Night Lights because the battery can overheat and cause the light to melt, posing a fire hazard.

    Product
    Circo Night Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V451000·2015-07-20

    Mazda Recalls 2007-2014 CX-9 Vehicles for Front Suspension Defect

    Mazda is recalling 2007-2014 CX-9 vehicles because front suspension ball joints may corrode, potentially causing loss of steering control and increasing crash risk.

    Product
    MAZDA — MAZDA CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E061000·2015-07-17

    SAF-Holland Recalls CBX Series Trailer Suspension Systems for Pivot Bolt Failure

    SAF-Holland is recalling CBX series trailer suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer and increasing crash risk.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V450000·2015-07-17

    BMW Recalls 2014-2015 MINI Cooper Models for Side Impact Defect

    BMW is recalling 2014-2015 MINI Cooper, Cooper S, and John Cooper Works vehicles because rear seats fail federal side impact safety standards, increasing injury risk.

    Product
    MINI — MINI JOHN COOPER WORKS, COOPER S, COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E062000·2015-07-17

    H&H Sports Protection Recalls VCAN V528 Milano Motorcycle Helmets

    H&H Sports Protection is recalling VCAN V528 Milano motorcycle helmets because the retention systems failed testing and required labeling is missing.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15T014000·2015-07-17

    Continental ContiProContact Tires Recalled for Bead Air Leak Defect

    Continental is recalling specific ContiProContact tires manufactured in early 2015 because a manufacturing error may cause air leaks from the bead area, increasing the risk of sudden tire failure and a crash.

    Product
    TIRES:BEAD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15742·2015-07-17

    EKO Recalls Motion Sensor Trash Cans Due to Laceration Hazard

    EKO is recalling motion sensor trash cans sold at Costco because a protective collar can dislodge, exposing a sharp edge that poses a laceration risk.

    Product
    Trash cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15187·2015-07-16

    Cash Acme Heatguard TAFR Devices Recalled Due to Scald Hazard

    Reliance Worldwide is recalling Cash Acme Heatguard TAFR devices because a thermal failure could cause scalding injuries. About 26,000 units are affected.

    Product
    Cash Acme Heatguard Temperature Actuated Flow Reducing (TAFR) Device
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1207-2015·2015-07-15

    SLIM-K Capsules Recalled for Unapproved Dangerous Ingredients

    Bethel Nutritional Consulting is recalling SLIM-K capsules because FDA testing found unapproved ingredients including sibutramine and phenolphthalein.

    Product
    SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1951-2015·2015-07-15

    Shiley Pediatric Tracheostomy Tubes Recalled for Breathing Difficulties

    FDA recalls Shiley tracheostomy tubes due to reports of patient discomfort and breathing difficulties.

    Product
    Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube with TaperGuard Cuff. Intended for use in providing tracheal access for airway managements.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1216-2015·2015-07-15

    Hospira Recalls Bupivacaine Hydrochloride Vials Due to Particulate Matter

    Hospira is recalling Bupivacaine Hydrochloride Injection vials because they contain free-floating and embedded iron oxide particles.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E060000·2015-07-15

    Flex-A-Lite Recalls Electric Fan Kits Due to Fire Risk

    Flex-A-Lite is recalling specific electric fan kits because missing fuse holders and insufficient circuit breakers may cause electrical damage and vehicle fires.

    Product
    ENGINE AND ENGINE COOLING:COOLING SYSTEM:FAN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1989-2015·2015-07-15

    Alliance Partners Recalls Nakoma-SL Cervical Plating Drill Guides

    Alliance Partners LLC is recalling 21 Nakoma-SL Anterior Cervical Plating System drill guides because screws may advance through the plate during implantation.

    Product
    Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for anterior intervertebral screw fixation of the cervical spine at levels C2-T1. The Nakoma ACP System is indicated for temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·15182·2015-07-15

    Cooper Lighting Recalls Fluorescent Fixtures Due to Fire Hazard

    Cooper Lighting is recalling about 1.62 million fluorescent fixtures because the sockets can overheat, arc, and melt, posing a fire hazard.

    Product
    Cooper Lighting, Portfolio and Utilitech fluorescent lighting fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide