The Recall Desk

State

Rhode Island product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40651–40675 of 76860

  • ModerateFDA (Devices)·Z-1241-2018·2018-04-04

    Encore Medical Recalls AltiVate Reverse Humeral Socket Shell Trials

    Encore Medical is recalling AltiVate Reverse Humeral Socket Shell Trials due to broken or missing screws and retaining clips.

    Product
    AltiVate Reverse INSTRUMENTATION, HUMERAL SOCKET SHELL TRIAL, STANDARD, REF 804-06-152, Qty: 01, Encore Medical, LP Orthopedic surgical instrument. Product Usage: The humeral socket shell trial is used to replicate/trial the shell geometry of the AltiVate Reverse Standard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1210-2018·2018-04-04

    Johnson & Johnson Recalls ACUVUE ADVANCE Contact Lenses Due to Foreign Matter

    Johnson & Johnson Vision Care is recalling specific lots of ACUVUE ADVANCE contact lenses because foreign matter was found between the blister package and foil.

    Product
    ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1272-2018·2018-04-04

    SIE AG Recalls FEMTO LDV Z8 Femtosecond Surgical Lasers

    SIE AG is recalling 125 FEMTO LDV Z8 femtosecond surgical lasers worldwide due to usability and performance improvements identified after a cataract procedure complication.

    Product
    The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser is an ophthalmic surgical laser intended for use in the creation of corneal incisions indicated for use in patients undergoing LASIK surgery, tunnel creation for implantation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0608-2018·2018-04-04

    Paddock Recalls Evamist Estradiol Spray Due to Vial Cracks

    Paddock Laboratories is recalling 52,596 bottles of Evamist (estradiol) transdermal spray because cracks in the vial neck may cause product evaporation, leaking, or dispensing failure.

    Product
    EVAMIST — EVAMIST (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1270-2018·2018-04-04

    Roche cobas e 411 Analyzer Recall for Questionable Results

    Roche Diagnostics is recalling cobas e 411 Immunoassay Analyzers because using 13 mm sample tubes without adapters may cause questionable results.

    Product
    cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical use), Catalog Numbers: 04775201001 (rack system), 04775279001 (disk system), 04775201973 (rack system) & 04775279973 (disk system).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2018·2018-04-04

    Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Labeling Error

    Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots were inadvertently commingled during manufacturing, potentially resulting in mislabeling.

    Product
    Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSVTB10.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1242-2018·2018-04-04

    Mindray Gas Module 3 monitoring spirometer recalled for regulatory changes

    Mindray DS USA is recalling 1,719 Gas Module 3 monitoring spirometers because the firm made multiple changes to the product requiring the submission of a new 510(k) premarket notification.

    Product
    Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device designed to monitor airway gases during anesthesia and/or assisted respiration. Monitored gases includes O2, CO2, N2O and anesthetic agents Halothane…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0613-2018·2018-04-04

    Akorn Recalls Subpotent Chlorhexidine Oral Rinse Kits

    Akorn, Inc. is recalling 24-HOUR Oral Care q4 Kits containing subpotent Chlorhexidine Gluconate Oral Rinse due to product crystallization.

    Product
    24-HOUR Oral Care q4 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0983-2018·2018-04-04

    PepsiCo Recalls Diet Pepsi Caffeine Free Due to Aspartame Labeling Error

    PepsiCo is recalling 194 cases of Diet Pepsi Caffeine Free because the outer packaging incorrectly states 'Aspartame Free' while the product contains aspartame.

    Product
    diet pepsi caffeine free Classic Diet Pepsi Taste, 12 FL OZ (355 mL), UPC: 0 12000 17230 4
    Category
    Food
    Distribution
    4 states
  • LowFDA (Drugs)·D-0605-2018·2018-04-04

    Renaissance Lakewood Recalls Flucanazole Injection Due to Stability Failures

    Renaissance Lakewood, LLC is recalling 1,277 bags of Flucanazole Injection due to superpotent and failed stability specifications.

    Product
    Flucanazole Injection, USP 200 mg in in 100 mL (2 mg/mL), 10 Single Dose Flexible Containers, Rx Only, Manufactured for: Claris Lifesciences, Inc. North Brunswick, NJ 08902 By; Claris Injectables Ltd. Gujarat, India --- NDC 36000-006-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V211000·2018-04-03

    Toyota Recalls 2017-2018 Models for Brake Booster Vacuum Pump Defect

    Toyota is recalling specific 2017-2018 Camry, Highlander, Sienna, Tacoma, and Lexus RX350 vehicles because a manufacturing defect in the brake booster vacuum pump may cause a sudden loss of brake assist.

    Product
    TOYOTA — TOYOTA, LEXUS SIENNA, TACOMA, RX350, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18135·2018-04-03

    3M Recalls Scotch Thermal Laminators Due to Overheating Burn Hazard

    3M is recalling about 395,000 Scotch thermal laminators because the plastic enclosure can overheat, posing a burn hazard. No injuries have been reported.

    Product
    Scotch™ thermal laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18133·2018-04-02

    Polaris Recalls RZR XP 1000 Vehicles Due to Exhaust Fire Hazard

    Polaris is recalling about 107,000 RZR XP 1000 vehicles because a cracked exhaust silencer can cause a fire. No injuries have been reported.

    Product
    Model Year 2014-2018 Polaris RZR XP 1000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V209000·2018-03-30

    Van Hool Recalls Motorcoaches Due to Seat Belt Buckle Casing Failure

    Van Hool is recalling 2015-2018 motorcoaches because seat belt buckle casings may fail, exposing the buckles and reducing the likelihood of seat belt use.

    Product
    VAN HOOL — VAN HOOL TX45, CX45, TD925, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V208000·2018-03-29

    Mercedes-Benz Recalls 2018 Models for Driver Air Bag Inflator Defect

    Mercedes-Benz is recalling 2018 AMG GT, AMG GT C, GLC43 AMG, GLC300, and GLC350e vehicles because defective steel in the driver-side air bag inflator housing may cause rupture during deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E, GLC 300, AMG GLC43, AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V203000·2018-03-29

    Alfa Romeo Stelvio Recall for Liftgate Wiring Water Leak

    FCA US LLC is recalling 2018 Alfa Romeo Stelvio vehicles because water leaks into liftgate wiring, causing corrosion that may allow the liftgate to open while driving.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V206000·2018-03-29

    Spartan Gladiator Recall for Front Axle Spindle Failure Risk

    Spartan Motors is recalling 2004-2007 Gladiator emergency response vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.

    Product
    SPARTAN — SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V199000·2018-03-29

    Navistar Recalls 2018-2019 International LT Trucks for Fuel Leak Risk

    Navistar is recalling 2018-2019 International LT trucks because a fender splash panel may rub against the fuel line, causing a leak that could lead to fire or crash.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E017000·2018-03-29

    Timoney Front Suspension Recall Due to Axle Spindle Fatigue Cracks

    Timoney Technology is recalling Mark 1 and Gen 2 Independent Front Suspensions because inconsistent machining may cause axle spindle failure and wheel separation.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V204000·2018-03-29

    Tesla Recalls Model S Vehicles Due to Steering Bolt Corrosion Risk

    Tesla is recalling 2012-2016 Model S vehicles because aluminum steering bolts may corrode and fracture, potentially causing a loss of power steering assist.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18733·2018-03-29

    Residential Elevators Recalls Traction Elevators Due to Impact Hazard

    Residential Elevators Inc. is recalling about 3,700 traction elevators installed in homes between January 2015 and April 2017 because the cab can rise unexpectedly to the top of the shaft, posing an impact hazard.

    Product
    Traction elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide