The Recall Desk

State

Rhode Island product recalls

73,833 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.

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58526–58550 of 76887

  • HighFDA (Food)·F-0498-2015·2014-11-19

    365 Organic Raisin Granola Recalled for Unlabeled Tree Nuts

    Whole Foods Market recalls 365 Organic Raisin Granola because it may contain pecans and coconut not listed on the label.

    Product
    365 Organic Raisin Granola in 17 ounce (482 gram) cardboard cartons; 12 cartons per case. UPC: 099482448738
    Category
    Food
    Distribution
    43 states
  • HighNHTSA·14E079000·2014-11-19

    AFX Recalls FX-76 Motorcycle Helmets for Impact Test Failure

    AFX North America is recalling specific FX-76 motorcycle helmets that failed federal impact tests. Riders may face serious injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0183-2015·2014-11-19

    Siemens Artis zeego C-arm systems recalled for cable routing defect

    Siemens is recalling 164 Artis zeego systems because a cable may be routed incorrectly, potentially causing system failure during procedures.

    Product
    Artis zeego systems, model number 10280959, with serial numbers 1000-1599 : Artis zeego is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0213-2015·2014-11-19

    Masimo SET uSpO2 Pulse Oximetry Cables Recalled for Crossed Wires

    Masimo Corporation is recalling specific SET uSpO2 Pulse Oximetry Cables due to crossed internal wires that may cause the monitoring device to display inverted SpO2 values.

    Product
    Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Cable is an in-line cable that provides continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (Sp02) and pulse rate when installed in a compatible OEM host system. Shipping/Package…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0185-2015·2014-11-19

    GE Healthcare Recalls Varicam and VG Hawkeye Nuclear Medicine Devices

    GE Healthcare is recalling 478 nuclear medicine imaging devices because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    GE Healthcare Varicam/VG and VG Hawkeye devices. Models H3000YA, H3000YB, H3000YC, H3000YD, H2508PA, H2508PB, H2508PC, H2508PD. Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0197-2015·2014-11-19

    Integra Titan Reverse Shoulder System Cutting Templates Recalled for Manufacturing Error

    Integra LifeSciences Corp. is recalling 12 units of Reverse Shoulder System cutting templates because the threaded handle was welded backwards, resulting in an incorrect cutting angle.

    Product
    Integra Titan Reverse Shoulder System right and left head cutting templates, 142.5 degrees. The Reverse Shoulder System Cutting Template, 142.5 degrees is an accessory for use with the Integra Titan Reverse Shoulder System. It is used to project the osteotomy angle on the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2015·2014-11-19

    Mondelez Recalls Chiclets Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    Chiclets Gum, 200 - 2 piece packs (400 pieces), Retail UPC 0 12546 02509 6, Case UPC 10012546108499
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0189-2015·2014-11-19

    GE Healthcare Recalls Brivo NM615 Nuclear Imaging Systems Due to Loose Fasteners

    GE Healthcare is recalling 22 Brivo NM615 nuclear imaging systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    Brivo NM615, is an all-purpose, single detector integrated nuclear imaging system. Models H3100TP, H3100TN, H3100TT, H3100TR, H3100TW, H3100WZ, H2401MP, H2401MN, H2401MT, H2401MR, H2401MW, H2401NJ. Product Usage: The Brivo NM 615 is an emission computed tomography system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0500-2015·2014-11-19

    Mondelez Recalls Chiclets Peppermint Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Peppermint Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    1) Chiclets Peppermint Gum, 6-10 piece packages (60 pieces), Retail UPC 0 12546 10105 9; 2)Chiclets Peppermint Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02501 0, Case UPC 1001254 3)Chiclets Peppermint Gum, (12 pieces), Retail UPC 0 12546 10128 8; 4)Chiclets…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0187-2015·2014-11-19

    GE Healthcare Recalls Discovery NM 630 Nuclear Imaging Systems

    GE Healthcare is recalling 147 Discovery NM 630 nuclear imaging systems to update maintenance procedures and prevent loose fasteners from causing parts to fall on patients.

    Product
    Discovery NM 630, dual detector free-geometry integrated nuclear imaging system. Models H3100RC, H3100RD, H2401LW. Product Usage: The GE Discovery NM 630 system is a medical tool intended for use by appropriately trained healthcare professionals to aid in detecting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2015·2014-11-19

    Roscoe Medical Recalls Transport Rollators Due to Caster Separation Risk

    Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.

    Product
    Transport Rollator with Padded Seat; Large 8-inch wheels with wheel locks (indoor and outdoor use), fold down footrests, ergonomic handles, curved padded backrest and handy wire basket for storage. Item# 30192 Burgundy each/Item# 30194 Blue each.. Transport Rollator is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0499-2015·2014-11-19

    Chiclets Gum Recalled for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Assorted Variety Multipak fruit flavor gum due to undeclared soy lecithin on the label.

    Product
    Chiclets Assorted Variety Multipak - Fruit Flavor Gum, 6-10 piece packages (60 pieces), 6 PAK, Retail UPC 0 12546 10102 8; 2)Chiclets Assorted Variety Multipak - Fruit Flavor Gum, 7-6 PAK packages (420 pieces), Retail UPC 0 12546 0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14T016000·2014-11-19

    Bluestar Trailer Tires Recalled for Sidewall Blister Risk

    China Manufacturers Alliance is recalling specific Bluestar trailer tires that may develop sidewall blisters, potentially causing loss of vehicle control.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0245-2015·2014-11-19

    Fougera Recalls Fluocinonide Gel Due to Residual Solvent Concerns

    Fougera Pharmaceuticals is recalling specific lots of Fluocinonide Gel USP, 0.05% because they may not meet USP requirements for residual solvents.

    Product
    FLUOCINONIDE GEL USP, 0.05%, Rx only, For External Use Only, Not For Ophthalmic Use, a) NET WT 15 gram tubes and b) NET WT 60 grams tubes, E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0135-15 (15 g) and NDC 0168-0135-60 (60 g)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0248-2015·2014-11-19

    Assured Naproxen Sodium Tablets Recalled Due to Mispackaging Error

    Contract Packaging Resources Inc. is recalling Assured Naproxen Sodium Tablets because correct labeled bottles of Assured Ibuprofen softgels were mistakenly packaged into Naproxen cartons.

    Product
    Assured Naproxen Sodium Tablets, USP 220 mg., 15 count bottle, Repackaged by Contract Packaging Resources, Inc 8009 Industrial Village Road Greensboro, NC 27409 Distributed by Greenbrier International, Inc Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0211-2015·2014-11-19

    Maquet Cardiohelp-I System Recalled for Potential Software Display Error

    Maquet Cardiovascular is recalling 331 Cardiohelp-I Systems due to a software issue that may display an erroneous 'Battery Needs Service' message after startup.

    Product
    Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide removal system used to pump blood thorough the extracorporeal bypass circuit for circulatory and/or pulmonary support during procedures requiring cardiopulmonary bypass (for periods up to six hours).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0198-2015·2014-11-19

    Zimmer Persona Stemmed 5 Degree Cemented Tibia Recalled for Cleaning Failure

    Zimmer, Inc. is recalling 138 units of Persona Stemmed 5 Degree Cemented Tibia knee components due to a cleaning process validation failure.

    Product
    Persona Stemmed 5 Degree Cemented Tibia Product Usage: This device is indicated for patients with severe knee pain and disability due to:  Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis.  Collagen disorders, and/or avascular necrosis of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0207-2015·2014-11-19

    CooperSurgical MILEX Pessary Kits Recalled for Incorrect Expiration Date

    CooperSurgical is recalling 17 MILEX Pessary Kits because the packaging displays an incorrect expiration date.

    Product
    CooperSurgical MILEX PESSARY KITS-Ring w/Support Folding Pessary- #1 Model: MXKPRS01 Product Usage: The CooperSurgical Milex silicon pessary is a safe and effective device used to manage a number of gynecologic issues including pelvic support defects and stress urinary…
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Devices)·Z-0208-2015·2014-11-19

    CooperSurgical MILEX Pessary Kits Recalled for Incorrect Expiration Date

    CooperSurgical is recalling 6 units of MILEX Pessary Kits due to incorrect expiration dates printed on the packaging.

    Product
    CooperSurgical MILEX PESSARY KITS- Hodge w/Support Folding Pessary- #1 Model: MXKPHS01 Product Usage: The CooperSurgical Milex silicon pessary is a safe and effective device used to manage a number of gynecologic issues including pelvic support defects and stress urinary…
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Drugs)·D-0247-2015·2014-11-19

    Fresenius Kabi Recalls Haloperidol Decanoate Injection Due to Impurity Failure

    Fresenius Kabi is recalling Haloperidol Decanoate Injection vials due to an out-of-specification impurity result. The recall covers 216,517 vials distributed nationwide and in Puerto Rico.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·079-2014-EXP·2014-11-18

    City Line Foods Recalls Pretzel Dogs for Undeclared Soy Allergen

    City Line Foods is expanding a recall of 1.2 million pounds of frozen pretzel dog products due to misbranding and undeclared soy lecithin, a known allergen.

    Product
    Pennsylvania Firm Expands Recalls Pretzel Dog Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·15027·2014-11-18

    CoScentrix Recalls DD Brand Candles Due to Fire Hazard

    CoScentrix is recalling approximately 256,000 DD brand candles sold at Hobby Lobby because the high flame can ignite the wax surface, posing a fire hazard.

    Product
    DD Brand Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V737000·2014-11-18

    Mack Trucks Recalls 2015 CHU and CXU Models for Steering Defect

    Mack is recalling 1,048 model year 2015 CHU and CXU trucks because incorrectly positioned tie rod collars may allow ball sockets to come loose, risking loss of steering.

    Product
    MACK — MACK CHU, PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide