The Recall Desk

State

Rhode Island product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35051–35075 of 76791

  • ModerateFDA (Drugs)·D-1313-2019·2019-06-05

    Inopak Recalls Inoderm Antiseptic Hand Soap Due to Manufacturing Deviations

    Inopak Ltd is recalling Inoderm Antiseptic Hand Soap because it was not produced under current good manufacturing practices.

    Product
    INODERM Antiseptic Hand Soap (E-2), .6% (incorrectly labeled on bags as 75%) PCMX, 800ml/27fl.oz.pouches (NDC 058575-110), 12 x 800 Bag-N-Box pouches per case (NDC 058575-110-80), 5014-404-NB; INOPAK, 24 Executive PKWY, Ringwood, NJ 07456.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1318-2019·2019-06-05

    Inopak Antibacterial Hand Soap Recalled for CGMP Deviations

    Inopak Ltd is recalling specific batches of Antibacterial Hand Soap because they were not produced under current good manufacturing practices.

    Product
    Antibacterial Hand Soap, .3% P.C.M.X, labeled as STYLE Antibacterial Hand Soap with moisturizers, a) 1000 ml pouches, 10/1000 ML. Large Valve pouches per case, 5031-404-LN, b) 1000 ml pouches, 8/1000 ML. Disc Pumps pouches per case, 5031-L1000, c) 800 ML Universal Valve pouches…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1686-2019·2019-06-05

    Teleflex Medical Recalls RUSCH LASERTUBE Due to Partial Foil Separation

    Teleflex Medical is recalling 2,325 units of RUSCH LASERTUBE (Rubber) because the laser guard foil partially separated or detached at the edges.

    Product
    RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1312-2019·2019-06-05

    Inopak Recalls Hand Sanitizer Due to Manufacturing Practice Deviations

    Inopak Ltd is recalling DermaGel and SaniTyze hand sanitizers because they were not produced under current good manufacturing practices.

    Product
    Instant Waterless Hand Sanitizer, Ethyl Alcohol, 62%, packaged as a) DermaGel Instant Waterless Hand Sanitizing Gel with Moisturizers, with Aloe Vera & Vitamin E, packaged in a) 1000 ml Disc Pump pouches (NDC 58575-340), 8 x 1000 ml Disc Pump pouches per case, Product Code…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1311-2019·2019-06-05

    Inopak Recalls AQUACIL Hand Sanitizer Due to Manufacturing Deviations

    Inopak Ltd is recalling specific batches of AQUACIL instant foaming hand sanitizer because they were not produced under current good manufacturing practices.

    Product
    AQUACIL instant foaming hand sanitizer, alcohol free formula, benzalkonium chloride 0.1% (w/w), packaged in a) 18 FL OZ (532 mL) bottles, 12/18OZ bottles per case, Product Code BIO-5075-432-02; b) 1000 ML pouches, 6/1000 ML pouches per case, Product Code BIO575-OS1000…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1317-2019·2019-06-05

    Inopak Recalls Sani-Guard-SF Foam Hand Sanitizer Due to Manufacturing Deviations

    Inopak Ltd is recalling Sani-Guard-SF Waterless Foam Hand Sanitizer because it was not produced under current good manufacturing practices.

    Product
    Sani-Guard-SF Waterless Foam Hand Sanitizer, Ethyl Alcohol 70%, packaged in a) 6/1000 ml pouches per case, 5068-FL1000, b) 1000 ml cartridge pouch, 6/1000 ml .8ml Option Cartridge pouches per case, 5068-OS1000, Inopak LTD
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V411000·2019-06-04

    Ferrari Recalls Multiple Models Due to Air Bag Control Module Malfunction

    Ferrari is recalling 893 vehicles because the air bag control module may malfunction, potentially causing air bags or seat belt pretensioners to fail to deploy or deploy improperly.

    Product
    FERRARI — FERRARI F12 BERLINETTA, CALIFORNIA T, 488 GTB, 488 SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19750·2019-06-04

    Polaris Recalls 2015-2019 Ranger EV Vehicles Due to Crash Hazard

    Polaris is recalling about 3,900 Ranger EV recreational off-highway vehicles due to a wiring defect that can cause unexpected acceleration and crashes.

    Product
    Model Year 2015 - 2019 Polaris RGR EV recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V412000·2019-06-04

    Honda Recalls 2018-2019 Motorcycles Due to Transmission Shaft Defect

    Honda is recalling specific 2018 and 2019 motorcycles because a transmission part may detach, causing gear misalignment that increases crash risk.

    Product
    HONDA — HONDA CB300R, CMX300, CRF250L, CBR300R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19131·2019-06-04

    Generation Brands Recalls Small Stratton Glass Pendant Light Fixtures

    Generation Brands is recalling Small Stratton glass pendant light fixtures because they can detach from the cord and fall, posing an injury risk.

    Product
    Small Stratton glass pendant light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19749·2019-06-04

    Polaris Recalls 2019 RZR XP 4 Turbo S Vehicles Due to Brake Failure

    Polaris is recalling about 1,200 Model Year 2019 RZR XP 4 Turbo S recreational off-highway vehicles because the brakes can fail, posing crash and injury hazards.

    Product
    Model Year 2019 Polaris RZR XP 4 Turbo S recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·064-2019·2019-05-31

    Perdue Recalls Chicken Products Due to Possible Bone Contamination

    Perdue Foods is recalling approximately 31,703 pounds of ready-to-eat chicken products that may contain pieces of bone material.

    Product
    PERDUE FOODS, LLC. — Perdue Foods LLC Recalls Perdue Simply Smart Organics Poultry Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·063-2019·2019-05-31

    Johnsonville Recalls Jalapeno Cheddar Sausage Due to Plastic Contamination

    Johnsonville is recalling ready-to-eat jalapeno cheddar smoked sausage links due to possible hard green plastic contamination. No adverse reactions have been reported.

    Product
    Johnsonville, LLC — Johnsonville, LLC. Recalls Ready-To-Eat Jalapeno Cheddar Smoked Sausage Links Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V406000·2019-05-30

    Jayco Recalls 2020 Greyhawk Motorhomes Due to Brake Valve Defect

    Jayco is recalling 2020 Greyhawk motorhomes because a defective brake relay valve may cause extended stopping distances, increasing crash risk.

    Product
    JAYCO — JAYCO GREYHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V403000·2019-05-30

    Mazda Recalls 2018 CX-9 Vehicles Due to Wiring Harness Defect

    Mazda is recalling 2018 CX-9 vehicles because a wiring harness defect may disable the passenger air bag, turn signals, or engine starting system.

    Product
    MAZDA — MAZDA CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E037000·2019-05-30

    Seats Incorporated Recalls ABTS 6-Way Seats Due to Weld Defect

    Seats Incorporated is recalling ABTS 6-way seats because poor weld penetration may cause the seat to move unexpectedly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19748·2019-05-30

    Excel Industries Recalls Zero-Turn Mowers Due to Fire Hazard

    Excel Industries is recalling about 5,400 zero-turn mowers because a wire tie could damage the fuel line, posing a fire hazard. No injuries have been reported.

    Product
    Zero turn lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1288-2019·2019-05-29

    Heritage Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium Tablets USP 100 mg 90 film coated tablets Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India. Manufactured for: Heritage Pharmaceuticals Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide