The Recall Desk

State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45376–45400 of 76871

  • HighCPSC·17744·2017-05-09

    Honda Recalls 2017 Pioneer 700 Vehicles Due to Seat Belt Defect

    American Honda is recalling about 2,200 2017 Pioneer 700 recreational off-highway vehicles because a manufacturing defect may cause the front passenger seat belt buckle to fail.

    Product
    Recreational off-highway vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V306000·2017-05-08

    Forest River Recalls 2017 XLR ToyHaulers for Incorrect Tire Pressure Label

    Forest River is recalling 2017 XLR ToyHauler trailers because the Federal Placard incorrectly lists rear tire pressure as 50psi instead of 80psi, which could lead to tire failure.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E023000·2017-05-05

    TRW Recalls Aftermarket Lower Ball Joints for Toyota Vehicles

    TRW is recalling aftermarket lower ball joints for Toyota 4Runner, Sequoia, and Tundra vehicles because a design defect could cause steering loss and increase crash risk.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·044-2017·2017-05-04

    Marcho Farms Recalls Veal, Beef, and Pork Products for E. Coli Risk

    Marcho Farms is recalling approximately 5,620 pounds of veal, beef, and pork products due to possible non-O157 Shiga toxin-producing E. coli contamination.

    Product
    Marcho Farms, Inc. — Marcho Farms, Inc. Recalls Veal, Beef and Pork Products Due to Possible Non-O157 Shiga Toxin-Producing E. Coli (STEC) Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17146·2017-05-04

    Combi USA Recalls Stroller and Car Seat Combos Due to Fall Hazard

    Combi USA is recalling about 1,000 Shuttle Travel Systems because the car seat can disengage from the stroller frame, posing a fall hazard to infants.

    Product
    Combi Shuttle Travel System (stroller and car seat combos)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V304000·2017-05-04

    Hino 338 Trucks Recalled for Incorrect Certification Labels

    Jim Reed's Truck Sales is recalling 2014-2016 Hino 338 trucks because certification labels fail to identify the final stage manufacturer, potentially hindering safety recall awareness.

    Product
    HINO — HINO 338
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0687-2017·2017-05-03

    Isomeric Pharmacy Recalls Phenylephrine and Tropicamide Ophthalmic Drops

    Isomeric Pharmacy Solution, LLC is recalling 5,165 bottles of Phenylephrine 2.5% and Tropicamide 1% ophthalmic drops due to a lack of assurance of sterility.

    Product
    Phenylephrine 2.5%, Tropicamide 1%, 15 mL Multi-Dose Ophthalmic (spelled Opthalmic) Drops in a bottle, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1300, barcode 3 70285 13001 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0683-2017·2017-05-03

    Isomeric Pharmacy Recalls Triamcinolone Acetonide Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Triamcinolone Acetonide 40 mg/mL, Lidocaine HCl 10 mg/mL , 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1020, barcode 3 70285 10201 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0677-2017·2017-05-03

    FDA Recalls Unapproved hCG Body Shaper Product for Contamination

    The FDA is recalling hCG Body Shaper because it was marketed without approval and contains human chorionic gonadotropin, making it an unapproved drug.

    Product
    hCG Body Shaper, Highly Purified Human Chorionic Gonadotrophin 5000 IU, Colloidal Silver B12, Stabilizers/Excipients, Not For Medical Use, Must Be Refrigerated, Distributed by HCG Body Shaper, St. Peters, MO
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1832-2017·2017-05-03

    HeartWare HVAD Pump Driveline Splice Kit Recall for Improved Repair

    Medtronic is notifying clinicians that an improved splice kit is available to replace the HeartWare HVAD Pump Driveline Splice Kit due to a safety issue.

    Product
    HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended to repair the driveline cable once an electrical break has been identified. These repairs are limited to the portion of the driveline that is outside the patient boundary (exit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V297000·2017-05-03

    Audi Recalls 2017 Q5 Vehicles Due to Gearbox Defect

    Volkswagen Group of America is recalling 2017 Audi Q5 vehicles because a gearbox defect may allow the vehicle to roll unexpectedly while in Park.

    Product
    AUDI — AUDI Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2158-2017·2017-05-03

    FDA Recalls Apple Cider Packed by Bevovations Due to Elevated Patulin Levels

    Bevovations, LLC is recalling specific apple cider products due to elevated levels of patulin. The recall covers 1,409 cases distributed in New Hampshire, Connecticut, Massachusetts, and Rhode Island.

    Product
    Apple Cider packed under the following labels: RUDY'S BLEND APPLE CIDER, 1 GAL. (3.78L), UPC: 8 56005 00344 3; RUDY'S BLEND APPLE CIDER; 1/2 GAL (1.89L), 8 56005 00434 6; FRESHLY PRESSED APPLE CIDER Carlson Orchards Harvard, Mass, 1/2 GAL (1.89L), 8 56005 00323 8; FRESHLY…
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·17V289000·2017-05-03

    Porsche Recalls Macan Models Due to Fuel Pump Flange Crack Risk

    Porsche is recalling 2015-2017 Macan models because a fuel pump flange may crack, causing a fuel leak that increases fire risk.

    Product
    PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN, MACAN GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0682-2017·2017-05-03

    Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,352 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Methylprednisolone Acetate 80 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1011, barcode 3 70285 10111 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0686-2017·2017-05-03

    Isomeric Pharmacy Recalls Testosterone Injection Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,156 vials of Testosterone Cypionate and Propionate injection due to production processes that cannot assure sterility.

    Product
    Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V298000·2017-05-03

    Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Crack Risk

    Volkswagen Group of America is recalling 2013-2017 Audi Q5 and Q7 vehicles because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.

    Product
    AUDI — AUDI Q5, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0685-2017·2017-05-03

    Isomeric Pharmacy Recalls Injection Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 851 vials of a multi-dose injection product because production processes cannot assure sterility.

    Product
    Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1101, barcode 3 70285 11013 9.
    Category
    Drug
    Distribution
    Distributed nationwide