The Recall Desk

State

Rhode Island product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53651–53675 of 76881

  • ModerateFDA (Devices)·Z-0147-2016·2015-10-28

    ConFormis iTotal Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS is recalling 110 units of the iTotal Posterior Stabilized Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT and ITOTAL PS-IPOLY-IMPLANT KIT-RIGHT Catalog Number:TPS1111111
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0137-2016·2015-10-28

    Biomet Thinflap System Cases Recalled Due to Lid Opening Difficulty

    Biomet Microfixation is recalling 5 Thinflap System Cases because the lids require excessive force to open.

    Product
    Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0134-2016·2015-10-28

    Synthes Recalls Spinal Pedicle Fixation Rods Due to Finishing Process Error

    Synthes (USA) Products LLC is recalling 492 spinal pedicle fixation rods because they were produced using a bead blast process not identified in the manufacturing specification.

    Product
    5.0mm Unit Rod 270mm, 5.0mm Unit Rod 290mm, 5.0mm Unit Rod 310mm, 5.0mm Unit Rod 330mm, 5.0mm Unit Rod 350mm, 5.0mm Unit Rod 370mm, 5.0mm Unit Rod 390mm, 5.0mm Unit Rod 410mm, 5.0mm Unit Rod 430mm, 5.0mm Unit Rod 450mm; Orthosis, Spinal, Pedicle fixation Intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0144-2016·2015-10-28

    ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 3 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - LEFT ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - RIGHT Catalog Number: TCR1111111
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0035-2016·2015-10-28

    JBN Chocolate Whey Protein Powder Recalled for Missing Milk Labeling

    Nutrition Resource Services is recalling JBN Chocolate Confidence Nutritional Support for Bariatric Surgery because the whey protein product is not labeled as containing milk.

    Product
    JBN (Just Be Natural) Chocolate Confidence Nutritional Support for Bariatric Surgery 25G 100% WHEY ISOLATE; NET WT. 43.4 oz. (2.7 lb) 1,230g - packaged in plastic bottles, UPC code: 655455018225, DIETARY SUPPLEMENT MANUFACTURED BY NRS -Nutrition Resource Services, Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0146-2016·2015-10-28

    ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 348 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConFormis iTotal CR Knee Replacement System- iTOTAL CR, Right Knee Catalog Number: M57250600020 (US) M5725INT0600020 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0153-2016·2015-10-28

    OneTray Sealed Sterilization Containers Recalled for Incorrect Labeling

    Innovative Sterilization Technologies LLC is recalling OneTray Sealed Sterilization Containers because the labels list the wrong steam sterilization time.

    Product
    OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization container used to steam sterilize medical devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0149-2016·2015-10-28

    Natus neoBLUE 3 Phototherapy System Recalled for Intensity Documentation

    Natus Medical is recalling 4,560 neoBLUE 3 Phototherapy systems because the instruction manuals did not accurately reflect the cleared intensity settings.

    Product
    Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy, Catalogue Part Number: 010066; Top Assembly Part Number: 001103
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0136-2016·2015-10-28

    Biomet Neuro Combo Set Case Lid Requiring Excessive Force Recalled

    Biomet Microfixation is recalling 37 Neuro Combo Set Cases because the lids require excessive force to open.

    Product
    Neuro Combo Set Case The cases hold surgical instrumentation in place during handling and storage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0140-2016·2015-10-28

    ConForMIS iUNI Knee Replacement Recalled for Ethylene Glycol Residue

    ConForMIS is recalling 6 units of the iUNI Unicondylar Knee Replacement System due to potential ethylene glycol residue.

    Product
    ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2, Right Lateral Catalog Number: M57220600240 (US) M5722INT0600240 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0139-2016·2015-10-28

    ConForMIS Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 71 units of the ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial due to potential small amounts of ethylene glycol residue.

    Product
    ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US) M5722INT0600210 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0053-2016·2015-10-28

    Donnatal Prescription Drug Recalled for Incorrect Ingredient Labeling

    Rx PAK is recalling Donnatal tablets because the label incorrectly lists Scopolamine Hydrocodone instead of Scopolamine Hydrobromide.

    Product
    DONNATAL — DONNATAL (PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V712000·2015-10-27

    Ford Recalls 2009-2010 Edge and Lincoln MKX for Fuel Tank Leak

    Ford is recalling 2009-2010 Edge and Lincoln MKX vehicles in 22 states and D.C. because salt water corrosion may cause the fuel tank to leak, increasing fire risk.

    Product
    FORD — FORD, LINCOLN EDGE, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V709000·2015-10-27

    Mercedes-Benz Recalls 2016 GLE450 and GLE63 Due to Drive Shaft Bolt Issue

    Mercedes-Benz is recalling 2016 GLE450 and GLE63 coupes because rear drive shaft bolts may loosen, causing the shaft to separate and the vehicle to stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE450, AMG GLE63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V711000·2015-10-27

    Mercedes-Benz Recalls Vehicles Due to Air Bag Control Unit Corrosion

    Mercedes-Benz is recalling 2008-2010 C300, C350, C63, and GLK350 vehicles because the air bag control unit may corrode and malfunction, potentially causing air bags to deploy unexpectedly or fail to deploy.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C63, GLK350, C300, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16018·2015-10-27

    LaRose Recalls Peanuts Flying Ace Ride-On Toys for Choking Hazard

    LaRose Industries is recalling Peanuts Flying Ace ride-on toys because blue hubcaps can detach, posing a choking hazard to young children.

    Product
    Peanuts Flying Ace Ride-On Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V710000·2015-10-27

    Ford Recalls 2016 E-350 and E-450 Vans for Trailer Brake Defect

    Ford is recalling 2016 E-350 and E-450 vans because the trailer brake controller may fail to actuate trailer brakes, increasing stopping distance and crash risk.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·132-2015·2015-10-26

    Adolf's Meat Products Recalls Assorted Deli Meat Due to Listeria Risk

    Adolf's Meat Products is recalling approximately 224 pounds of assorted deli meats produced in October 2015 due to possible Listeria monocytogenes contamination.

    Product
    Adolf's Meat Products — Adolf's Meat Products Recalls Assorted Deli Meat Due to Possible Listeria Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V701000·2015-10-26

    GM Recalls 1997-2004 Vehicles Due to Exhaust Fire Risk

    General Motors is recalling specific 1997-2004 Chevrolet, Buick, Pontiac, and Oldsmobile vehicles because engine oil may drip onto the hot exhaust manifold, posing a fire risk.

    Product
    CHEVROLET — CHEVROLET, BUICK, PONTIAC IMPALA, LUMINA, REGAL, MONTE CARLO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V705000·2015-10-26

    Volkswagen Recalls 2015-2016 Models for Brake Assist Loss Risk

    Volkswagen is recalling 2015-2016 Jetta, Beetle, Passat, and Golf vehicles because a camshaft lobe may shear off, causing a loss of brake assist.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, BEETLE, PASSAT, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V703000·2015-10-26

    Terex Advance Concrete Mixers Recalled for Steering Pump Failure

    Terex Advance is recalling 288 model year 2011-2015 concrete mixers because steering gear pumps may fail, reducing steering ability and increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE MIXER FD7000B, MIXER FD5000B, MIXER FD4000B, MIXER FD6000B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V704000·2015-10-26

    Isuzu Recalls 2006-2008 Trucks for Fuel Tank Corrosion and Leak Risk

    Isuzu is recalling 2006-2008 Chevrolet, GMC, and Isuzu trucks because the fuel tank may corrode and leak, increasing fire risk.

    Product
    CHEVROLET — CHEVROLET, GMC, ISUZU W4500, W3500, NPR, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V706000·2015-10-26

    Pierce Recalls 2015-2016 Models Due to Loose Front Drive Axle Hex Nuts

    Pierce is recalling 2015-2016 Arrow XT, Velocity, Enforcer, and Saber vehicles because front drive axle hex nuts may be loose, risking loss of propulsion.

    Product
    PIERCE — PIERCE ENFORCER, ARROW XT, VELOCITY, SABER
    Category
    Vehicle
    Distribution
    Distributed nationwide