The Recall Desk

State

Rhode Island product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34101–34125 of 76790

  • HighFDA (Devices)·Z-2130-2019·2019-08-07

    Burlington Medical Recalls Thyroid Collars Due to Inadequate Radiation Protection

    Burlington Medical is recalling 23 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially increasing health risks for users.

    Product
    Thyroid Collar Oversize, Product Number TS3, Part Numbers RBTS3-R, RETS3-R, RLTS3-R, RLTS3-SEP, RLTS3-T2T Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2086-2019·2019-08-07

    Teleflex Recalls Rusch EasyCath Kits Due to Sterility Concerns

    Teleflex Medical is recalling 3,700 Rusch EasyCath Kits because they may not be sterile. The kits were distributed nationwide to eight states.

    Product
    Rusch EasyCath Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2112-2019·2019-08-07

    Burlington Medical Recalls 310 Full Wrap Vests and Kilts for Radiation Protection Defects

    Burlington Medical is recalling 310 two-piece full wrap vests and kilts because the protective material may provide inadequate shielding against scatter radiation.

    Product
    2 pc Full Wrap Vest & Kilt, Product Number VK, Part Numbers ECREVKA, ECREVKB, ECREVKC, ECREVKXLM, ECSEVKA, ECSEVKB, ECSEVKC, ECSEVKXLM, REVK*F, REVK*M, REVKB, REVKC, REVKE, REVKXXLM, SEVK*F, SEVK*M, SEVKB, SEVKC, SEVKE, SEVKF, SEVKG, SEVKXLF, SEVKXXLM, UEVK*F, UEVK*M, UEVKXXLF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2099-2019·2019-08-07

    Inovo Single Luman Conserver Recalled for Potential Pressure Gauge Dislodgement

    Inovo, Inc. is recalling 690 Single Luman Conservers because the pressure gauge may dislodge from the mount, creating a leak.

    Product
    Inovo Single Luman Conserver Product Usage: This device is intended to regulate the flow of oxygen from an oxygen tank and only deliver oxygen as the patient inhales, resulting in greater efficiency and cost saving ratios.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2119-2019·2019-08-07

    Burlington Medical Recalls Thyroid Collars Due to Inadequate Radiation Protection

    Burlington Medical is recalling 210 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to increased health risks.

    Product
    Thyroid Collar, Magnetic Closure, Product Number TS5, Part Numbers RBTS5-R, RBTS5-T2T, RLTS5-R, RLTS5-T2T, SLTS5-R Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1578-2019·2019-08-07

    ImprimisRx Recalls Subpotent Timolol-Latanoprost Ophthalmic Drops Nationwide

    ImprimisRx NJ is voluntarily recalling 405 bottles of Timolol-Latanoprost P-F ophthalmic drops because the medication was found to be subpotent.

    Product
    Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops, packaged in 5mL bottles, Rx only, ImprimisRX NJ 1705 Route 46 West, Suite 4, Ledgewood, NJ 07852 (844) 446-6979
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2019·2019-08-07

    Burlington Medical Recalls Radiation Protection Kilts Due to Inadequate Shielding

    Burlington Medical is recalling 37 radiation protection kilts because the protective material may provide inadequate shielding against scatter radiation.

    Product
    Kilt, Single Item, Product Number Kilt, Part Numbers ECREKILTF, ECREKILTXLF, REKILTA, REKILTB, REKILTXLF, REKILTXLM, REKILT*M, SEKILTB, SEKILTC, SEKILT*F, SEKILT*M Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2056-2019·2019-08-07

    Agfa DR 800 Digital Radiography System Recalled for Image Mismatch

    Agfa N.V. is recalling four DR 800 digital radiography systems because the exposed area of fluoroscopic exams may not match the active detector area.

    Product
    AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following an anatomies/procedures: positioning fluoroscopy…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2098-2019·2019-08-07

    A&E Medical Ultra-Flex Pacing Wire Recalled for Instruction Updates

    Alto Development Corp is recalling Ultra-Flex MYO/Wire pacing wires to update instructions for use to ensure consistency with the M-21 loop electrode.

    Product
    A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire Looped Electrode (M-21 SERIES)- Temporary Pacing Electrode as follows: 021-001 MYO/Wire Ultra-Flex Monopolar (Wht.,2-0) 021-010 MYO/Wire Ultra-Flex Monopolar (Org.,2-0) 021-011 MYO/Wire Ultra-Flex…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1565-2019·2019-08-07

    Lupin Recalls Kaitlib Fe Tablets Due to Stability Test Failures

    Lupin Pharmaceuticals is recalling Kaitlib Fe chewable tablets because long-term stability testing showed out-of-specification impurities or degradation.

    Product
    Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets (0.8 mg/0.025 mg) and Ferrous Fumarate, Chewable Tablets, Rx Only, Distributed by: Lupin Pharmaceuticals, Inc. Baltimore, MD - 21202 Manufactured by: Lupin Limited Pathampur -454775 India. NDC 68180-903-11 (wallet…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1997-2019·2019-08-07

    Philips Recalls Azurion X-ray Systems Due to Software Defect

    Philips is recalling 229 Azurion Interventional Fluoroscopic X-ray Systems because a software defect may cause radiation levels too low for diagnostic images.

    Product
    Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1742-2019·2019-08-07

    Piramal Recalls Gablofen Baclofen Injection Due to Unknown Impurity

    Piramal Critical Care is recalling Gablofen (baclofen injection) due to the presence of an unknown impurity observed during shelf life.

    Product
    GABLOFEN — GABLOFEN (BACLOFEN INJECTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2133-2019·2019-08-07

    Xhale Assurance Nasal SpO2 Sensor Recall for Missing Instructions

    Xhale Assurance is recalling 701,272 Nasal Alar SpO2 Sensors because the Instructions for Use are missing steps for checking and changing the application site.

    Product
    Nasal Alar SpO2 Sensor, Adult/Pediatric SpO2 Sensor, Rx Only Product Usage: The Assurance¿ Nasal Alar SpO2 Sensor is indicated for single patient use for continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate from the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V578000·2019-08-06

    Altec Recalls 2018-2019 Aerial Devices Due to Fastener Failure Risk

    Altec Industries is recalling 2018-2019 aerial devices because high-strength fasteners may fail, potentially causing the pedestal to separate from the turntable.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19766·2019-08-06

    BRP Recalls 2017-2018 Ski-Doo Snowmobiles Due to Fuel Leak and Fire Hazard

    BRP is expanding a recall for 2017-2018 Ski-Doo snowmobiles because the fuel delivery system can leak, posing a fire hazard. No injuries have been reported.

    Product
    2017 Ski Doo MXZ, Summit and Renegade snowmobiles and 2018 MXZ and Renegade snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V579000·2019-08-06

    BMW Recalls 2008-2012 Models for Blower Wiring Fire Risk

    BMW is recalling 2008-2012 128i, 135i, and 135is vehicles because blower-regulator wiring may overheat and cause a fire. Owners should contact dealers for a free inspection and replacement.

    Product
    BMW — BMW 135I, 128I, 135IS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V577000·2019-08-06

    KME Fire Trucks Recalled for Front Shock Separation Risk

    KME is recalling specific 2018-2019 Predator fire trucks because front shocks may separate, potentially causing a loss of power steering assist and increasing crash risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR TDA, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V576000·2019-08-06

    Toyota Recalls 2019 RAV4 Models for Backup Camera Defect

    Toyota is recalling 2019 RAV4 and RAV4 Hybrid vehicles because a damaged electrical connector may prevent the backup camera from activating, increasing crash risk.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V573000·2019-08-05

    Altec Recalls 2017-2019 LS60 Aerial Devices for Stability Defects

    Altec Industries is recalling 2017-2019 LS60 Aerial Devices because they may not meet stability requirements, creating a risk of overturning and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V575000·2019-08-05

    Ford Recalls 2020 Explorer and Lincoln Aviator for Parking Brake Cover Issue

    Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a missing parking brake cover or Factory Mode setting may allow the vehicle to roll away or hide gear selection.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V574000·2019-08-05

    Harley-Davidson Recalls Touring Motorcycles for Missing Rear Reflectors

    Harley-Davidson is recalling specific Touring and CVO Touring motorcycles because a luggage conversion kit removed rear red reflectors without providing replacements, reducing visibility.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLTRUSE, FLHTK, FLHTCUL, FLHTKSE
    Category
    Vehicle
    Distribution
    Distributed nationwide