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.

Which agencies issued them

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.

56876–56900 of 76887

  • SevereFDA (Food)·F-1921-2015·2015-04-15

    Nutiva Coconut Treats Recalled Due to Salmonella Contamination in Coconut Flakes

    Nutiva is recalling O'Coconut Lightly Sweetened Coconut Treats because desiccated coconut flakes used in the product tested positive for Salmonella.

    Product
    Nutiva O'Coconut Lightly Sweetened Coconut Treat - Hemp & Chia. Sold in Singles of 24 - 0.5 oz, per box - 6-92752-10502-9 24 singles x 6 caddies per shipping case - 144 individual units per case. Certified Organic, Fair Trade Certified. Manufactured for: Nutiva, 213 W.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1929-2015·2015-04-15

    Classic Cooking Kale and Quinoa Cake Recalled for Undeclared Peanut

    Classic Cooking LLC is recalling Kale and Quinoa Cake because it contains undeclared peanut protein, a major allergen.

    Product
    classic cooking Kale and Quinoa Cake, NET WT. 6.75 lbs. UPC 7-4863-32511-8. KEEP FROZEN.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V223000·2015-04-15

    Chrysler Recalls 2015 Ram ProMaster City for Side Air Bag Defect

    Chrysler is recalling 2015 Ram ProMaster City vehicles because side air bag curtains may not deploy properly, increasing injury risk in crashes.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V225000·2015-04-15

    GM Recalls 2004-2007 Cadillac CTS-V for Brake Hose Corrosion

    General Motors is recalling 2004-2007 Cadillac CTS-V vehicles in specific states because front brake hose fittings may corrode, potentially causing brake leaks and increased stopping distance.

    Product
    CADILLAC — CADILLAC CTS-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1377-2015·2015-04-15

    Carestream CS 8100 X-ray Device Recalled for Unexpected Head Descent

    Carestream Health is recalling CS 8100 panoramic X-ray units because the device head may descend unexpectedly. Approximately 3,110 units were distributed worldwide.

    Product
    CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic digital panoramic X-ray images to be used at the direction of healthcare professionals of the dento-maxillo-facial region of the human anatomy as diagnostic…
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-1404-2015·2015-04-15

    Teleflex Medical Recalls Pluer-evac Sahara Chest Drainage Systems

    Teleflex Medical is recalling 2,148 adult-sized Pluer-evac Sahara Chest Drainage Systems because they contain infant-sized components.

    Product
    Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Drugs)·D-0483-2015·2015-04-15

    Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization

    Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection due to crystallization. The recall covers vials distributed nationwide and internationally.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·15V222000·2015-04-15

    Chrysler Recalls 2006 Dodge Viper and Jeep Models for Clutch Defect

    Chrysler is recalling 2006 Dodge Viper and Jeep Wrangler/Liberty vehicles because a broken clutch pedal spring may cause the vehicle to lurch unexpectedly, increasing crash risk.

    Product
    DODGE — DODGE, JEEP VIPER COUPE, LIBERTY, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15728·2015-04-15

    Cycle Gear Recalls Wheelies Toys Due to Excessive Lead Levels

    Cycle Gear is recalling Wheelies semi-truck and motorcycle toys because they contain excessive lead levels, violating federal standards.

    Product
    Wheelies semi-truck with six motorcycles and push-along motorcycle with rider.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15110·2015-04-15

    Husky Vertical Bike Hooks Recalled Due to Risk of Injury

    Waterloo Industries is recalling Husky Securelock Vertical Bike Hooks because they can detach and fall, posing a risk of injury to bystanders.

    Product
    Husky® Securelock™ Vertical Bike Hooks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1397-2015·2015-04-15

    CooperSurgical Infant Transport Mattress Recalled for Missing Expiration Date

    CooperSurgical is recalling TransWarmer Infant Transport Mattresses because they lack expiration dates, potentially failing to meet specifications.

    Product
    CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421 Private label: NovaPlus TransWarmer Infant Heat Therapy Mattress with WarmGel. P/N V6390 Provides warmth during transport of infant within the hospital or between hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1942-2015·2015-04-15

    Vitarroz Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Vitarroz Sazon seasoning packets because the cumin ingredient may contain undeclared peanut protein.

    Product
    VITARROZ SAZON CON CULANTRO Y ACHIOTE CORIANDER & ANNATTO, NET WT. 6.34 OZ. 180g, Jumbo SOBRES 36 PACKETS, UPC 0 72670 04255 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0482-2015·2015-04-15

    Hospira Recalls Ketorolac Tromethamine Injection Due to Crystallization

    Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection because of crystallization. The affected vials were distributed nationwide and in Guam and Singapore.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1941-2015·2015-04-15

    Iberia Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Sazon Iberia seasoning because it may contain undeclared peanut protein. Consumers should check lot numbers and stop using the product.

    Product
    SAZON IBERIA CON CULANTRO Y ACHIOTE Coriander & Annatto: 1) NET WT. 3.52 OZ. 100g, 18/20 PACKS, UPC 0 75669 10832 9, 2) NET WT. 6.34 OZ. 180g, 15/36 PACKS, UPC 0 75669 10831 2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2015·2015-04-15

    Carestream CS 8100 3D Dental X-Ray Devices Recalled for Unexpected Head Descent

    Carestream Health is recalling 470 CS 8100 3D dental X-ray units because the device head may descend unexpectedly, posing a risk of injury to patients or operators.

    Product
    CS 8100 3D, CATALOG # (s): 5311162, 5311188. Intended to produce complete or segmented tomographic digital panoramic X-ray images and three-dimensional digital X-ray images of the dentomaxillo-facial area to be used at the direction of healthcare professionals as diagnostic…
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1394-2015·2015-04-15

    Toshiba INFX-8000V Interventional Angiography System Recall for Brake Defect

    Toshiba is recalling 28 INFX-8000V Interventional Angiography Systems because the table base rotational brake may not engage when force is applied to the table top.

    Product
    INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V224000·2015-04-15

    Thor Motor Coach Recalls 2016 Motorhomes for Missing Weight Label

    Thor Motor Coach is recalling 168 model year 2016 motorhomes because the Occupant and Cargo Carrying Capacity label may be missing water weight information, creating an overload risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR CHATEAU, OUTLAW, CITATION, SIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2015·2015-04-15

    VasoNova Vascular Positioning System G4 Console Recalled for Standard Noncompliance

    VasoNova is recalling 17 Vascular Positioning System G4 Consoles due to noncompliance with IEC Standard 60101-1-1.

    Product
    VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and Console are indicated for guidance and tip positioning for central venous catheters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1379-2015·2015-04-15

    TEM Systems Recalls ROTROL P Control Vials Due to Partial Filling

    TEM Systems Inc is recalling specific lots of ROTROL P Control vials because some were found to be partially filled.

    Product
    ROTROL P Control for ROTEM delta Thromboelastometry System, Manufactured for: Tem Innovations GmbH.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0436-2015·2015-04-15

    Heritage Pharmaceuticals Recalls Gliptizide and Metformin Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling specific lots of Gliptizide and Metformin HCL tablets because they failed impurity specifications. The affected bottles were distributed nationwide.

    Product
    GLIPIZIDE AND METFORMIN HCL — GLIPIZIDE AND METFORMIN HCL (GLIPIZIDE AND METFORMIN HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0435-2015·2015-04-15

    Mylan Recalls Fexofenadine HCl Tablets Due to Impurity Failures

    Mylan Pharmaceuticals is recalling specific lots of Fexofenadine HCl 60 mg tablets because they failed impurity specifications. The recall covers 13,856 bottles distributed nationwide.

    Product
    Fexofenadine HCl Tablets, USP, 60 mg, Allergy, Antihistamine, Indoor and Outdoor Allergies, Non-Drowsy, Original Prescription Strength, a) 60 count Bottles, NDC 0378-0781-91, b) 500 count Bottles, NDC 0378-0781-05, Manufactured by: Mylan Pharmaceuticals Inc, Morgantown, WV…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D00432-2015·2015-04-15

    Qualitest Recalls Promethazine VC With Codeine Syrup Due to Impurity

    Qualitest Pharmaceuticals is recalling Promethazine VC with Codeine Syrup because a stability lot failed impurity specifications.

    Product
    PROMETHAZINE VC WITH CODEINE SYRUP, EACH 5 ml contains: Codeine Phosphate 10 mg, Promethazine Hydrochloride 6.25 mg, Phenylephrine Hydrochloride 5 mg, alcohol 7%, (a) 4 fl oz bottle (NDC 0603-1588-54) and (b) 16 fl oz bottle (NDC 0603-1588-58) Rx only, Manufactured for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V219000·2015-04-14

    Gillig Recalls 2013-2015 Low Floor Buses Due to Brake Hose Wear

    Gillig is recalling 623 Low Floor transit buses from 2013-2015 because brake hoses may rub against suspension towers, potentially causing air leaks and increased stopping distances.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2015·2015-04-14

    Beech-Nut Recalls Baby Food Jars Due to Possible Glass Contamination

    Beech-Nut Nutrition is recalling approximately 1,920 pounds of Stage 2 sweet potato and chicken baby food jars due to possible glass contamination.

    Product
    Beech-Nut Nutrition Corporation — Beech-Nut Nutrition Recalls Baby Food Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide