The Recall Desk

State

Rhode Island product recalls

73,576 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,048
Critical
221
Severe
707
Most recent
2026-10-21

Of the 3,048 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 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25651–25675 of 76624

  • ModerateFDA (Devices)·Z-1677-2021·2021-06-02

    Nobel Biocare Procera Recalls Two Dental Implant Crowns for Specification Defects

    Nobel Biocare Procera LLC is recalling two dental implant crown units because they were not manufactured to specification. The affected units were distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics Material Number: 77339
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0392-2021·2021-06-02

    Ascend Recalls Olmesartan Medoxomil Tablets Due to Foreign Tablet Presence

    Ascend Laboratories LLC is recalling 34,296 bottles of Olmesartan Medoxomil 20 mg tablets because they may contain a foreign tablet or capsule.

    Product
    OLMESARTAN MEDOXOMIL — OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0599-2021·2021-06-02

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets due to the presence of degradation impurities.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V409000·2021-06-01

    Altec Aerial Devices Recalled for Boom Spool Shift Risk

    Altec is recalling 2005-2021 aerial devices because boom spools can shift, increasing injury risk. Owners should contact Altec for free repairs.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V408000·2021-06-01

    Custom Truck Recalls 2020 Ford F-550 Vehicles Due to Display Defect

    Custom Truck is recalling 2020 Ford F-550 vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V407000·2021-05-29

    Ford Recalls 2021 F-150 Trucks Due to Steering Gear Defect

    Ford is recalling 2021 F-150 vehicles because internal steering gear damage could cause loss of steering control. Owners should not drive until the repair is complete.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V406000·2021-05-28

    2021 Mercedes-Benz Cabriolets: Rear Headrests May Be Incorrectly Mounted

    Mercedes-Benz USA is recalling approximately 218 2021 Cabriolet models due to rear headrests that may be incorrectly mounted to the seatbacks. The headrests could move or detach during a crash, increasing the risk of injury.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, E 450, AMG E53, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V403000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Water Intrusion Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because water may enter the foot wells, potentially causing electrical damage, engine stalls, or a blank instrument cluster.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V405000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Air Bag Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because the front passenger air bag may tear upon deployment, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V404000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 for Side Air Bag Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because side curtain air bags may not deploy properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V401000·2021-05-27

    BMW Recalls 3 Series Vehicles for Air Bag Inflator Defect

    BMW is recalling 1999-2001 3 Series vehicles because the driver-side air bag inflator may explode or underinflate, posing a risk of serious injury.

    Product
    BMW — BMW 330CI, 3 SERIES, 328CI, 330I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V402000·2021-05-27

    2021 INFINITI QX50 Steering Knuckle Structural Defect - Multiple Models Affected

    Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.

    Product
    INFINITI — INFINITI, NISSAN QX60, MURANO, Q50, GT-R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V400000·2021-05-27

    Triple E RV Recalls 2020-2021 Models Due to Refrigerator Exhaust Deflector Issue

    Triple E Recreational Vehicles is recalling 2020-2021 Serenity, Unity, and Wonder models because a low-positioned metal deflector allows exhaust to char the wood frame, increasing fire risk.

    Product
    TRIPLE E RV — TRIPLE E RV, TRIPLE E WONDER, SERENITY, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V398000·2021-05-27

    RAM 3500, 4500, and 5500 vehicles recalled for wheel stud failure

    Chrysler is recalling RAM trucks because incorrect manual torque specifications can cause wheel studs to over-tighten, break, and lead to wheel separation and possible crashes.

    Product
    RAM — RAM, DODGE 5500, 3500, 4500, RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21751·2021-05-27

    Umbrosa Pool and Patio Umbrellas Recalled Due to Arm Breakage Hazard

    Umbrosa is recalling about 250 pool and patio umbrellas because the arm can break at the elbow while in use, posing an injury hazard.

    Product
    Umbrosa umbrellas equipped with the Umbrosa Evolution Arm/Holder
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21750·2021-05-27

    Williams Advanced Materials Recalls Three Chemicals for Packaging and Labeling Violations

    Williams Advanced Materials & Chemicals is recalling sodium hydroxide, heptane, and naphtha because the packaging is not child-resistant and labels violate federal requirements.

    Product
    Williams Advanced Materials & Chemicals Recalls Three Chemical Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement (Recall Alert)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0503-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Isolate for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE NEOPOLITAN ICE CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 8 11836 02251 3 & 5lb, UPC 8 11836 02252 0 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • CriticalFDA (Food)·F-0539-2021·2021-05-26

    Natural Way Almond Butter Recalled for Potential Undeclared Peanuts

    Simkins Brothers Sweets is recalling Natural Way Almond Butter due to potential undeclared peanuts. Consumers should check for lot #505721.

    Product
    Natural Way Almond Butter 16 oz. UPC 850001775175 packaged in clear plastic jars
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0501-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89001 0 & 5lb, UPC 6 49241 87831 5 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereNHTSA·21V392000·2021-05-26

    Freightliner Recalls 2019 M2 Business Class Vehicles for Electrical Defect

    Daimler Trucks North America is recalling 2019 Freightliner M2 Business Class vehicles with 14Xe ePowertrains because insufficiently crimped stator wires may cause overheating and loss of drive power.

    Product
    FREIGHTLINER — FREIGHTLINER M2 BUSINESS CLASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1641-2021·2021-05-26

    Biopsybell 11G Direct Single Delivery Kits Recalled for Sterility Concerns

    Biopsybell is recalling 160 units of 11G Direct Single Delivery kits because they were labeled as sterile but may not have been sterilized.

    Product
    11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES), CODE INTVMN-SCDK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0376-2021·2021-05-26

    Teva Recalls Methylprednisolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Methylprednisolone Acetate Injectable Suspension due to a lack of assurance of sterility.

    Product
    Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, 10 mL Multiple Dose Vial, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-0045-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1644-2021·2021-05-26

    Biopsybell 11G Direct Single Access Devices Recalled for Sterility Concerns

    Biopsybell is recalling 50 units of 11G Direct Single Access devices labeled as sterile but potentially not sterilized, distributed in Mississippi and Kentucky.

    Product
    11G DIRECT SINGLE - ACCESS, CODE INTVMN-DSBAK
    Category
    Medical Device
    Distribution
    Distributed nationwide