The Recall Desk

State

Rhode Island product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31576–31600 of 76787

  • HighCPSC·20061·2020-01-29

    Delta Recalls Incline Sleepers for Newborns Due to Suffocation Risk

    Delta Enterprise Corp. is recalling about 5,900 incline sleepers for newborns to prevent the risk of suffocation. Consumers should stop using the products immediately.

    Product
    Beautyrest Beginnings Incline Sleeper with Adjustable Feeding Position for Newborns; Disney Baby Minnie Mouse Incline Sleeper with Adjustable Feeding Position for Newborns; Delta Children Deluxe 3-in-1 Activity Rocker, Feeder and Sleeper; Simmons Kids Beautyrest Deluxe 3-in-1…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20062·2020-01-29

    Graco Recalls Little Lounger Rocking Seats to Prevent Suffocation Risk

    Graco is recalling Little Lounger Rocking Seats to prevent the risk of infant suffocation. Consumers should stop using the product and contact Graco for a refund.

    Product
    Graco Little Lounger Rocking Seat
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0828-2020·2020-01-29

    Medicrea Pass LP Blunt K-wire Recalled for Incompatibility with Screws

    Medicrea International is recalling 190 units of Pass LP Blunt K-wires because they may not fit into Conical Cannulated Screws.

    Product
    Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0831-2020·2020-01-29

    Siemens ADVIA Centaur Folate Test Kits Recalled for Potential Cross-Reactivity

    Siemens is recalling 3,627 ADVIA Centaur Folate test kits because homocysteine assays may cause elevated folate results.

    Product
    Siemens ADVIA Centaur Folate (500 Test Kit Reference)- for IVD of folate in serum or red blood cell SMN: 10331250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0827-2020·2020-01-29

    Medicrea Pass LP Trocar K-wire Recalled for Fit Issues

    Medicrea International is recalling 30 units of Pass LP Trocar K-wires because they may not fit into conical cannulated screws.

    Product
    Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product reference : A06010130
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0801-2020·2020-01-29

    Hikma Recalls Methylprednisolone Sodium Succinate Injection Due to Labeling Error

    Hikma Pharmaceuticals is recalling 4,840 vials of Methylprednisolone Sodium Succinate Injection because the label incorrectly instructs healthcare professionals to reconstitute the product with 16 mL instead of 8 mL.

    Product
    METHYLPREDNISOLONE SODIUM SUCCINATE — METHYLPREDNISOLONE SODIUM SUCCINATE (METHYLPREDNISOLONE SODIUM SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0829-2020·2020-01-29

    Siemens ADVIA Centaur Folate 100 Test Kits Recalled for Elevated Results

    Siemens is recalling 12,796 ADVIA Centaur Folate 100 test kits because homocysteine assays may cause elevated folate results.

    Product
    Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate in serum or red blood cells SMN:10310308
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0799-2020·2020-01-29

    FDA Recalls NETSPOT Kits Due to Defective Aluminum Cap Crimp

    Advanced Accelerator Applications USA, Inc. is recalling NETSPOT kits because the dilution buffer vial has a loose aluminum cap crimp.

    Product
    NETSPOT — NETSPOT (68GA-DOTATATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0818-2020·2020-01-29

    Greiner Bio-One Recalls Damaged Vacuette Blood Collection Tubes

    Greiner Bio-One is recalling 1,002,000 Vacuette tubes that may have cap sealing damage, potentially causing vacuum loss and improper blood volume collection.

    Product
    VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles are use together as a system for the collection of venous blood. VACUETTE tubes are used to collect, transport, and process blood for testing serum, plasma, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V047000·2020-01-28

    Mercedes-Benz Recalls 2019 AMG GT63 Models Due to Wiring Harness Issue

    Mercedes-Benz is recalling 2019 AMG GT63 and GT63S vehicles because a transmission wiring harness may chafe against the drive shaft, potentially causing an engine stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT 63, AMG GT63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V048000·2020-01-27

    Mercedes-Benz Recalls AMG Models Due to Turbocharger Oil Leak Fire Risk

    Mercedes-Benz is recalling certain 2018-2019 AMG vehicles because a turbocharger oil feed line may leak, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT63, AMG S63, AMG E63S, AMG GT 63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V043000·2020-01-24

    Chrysler Recalls 2019-2020 Ram 2500 and 3500 for Fire Risk

    Chrysler is recalling 2019-2020 Ram 2500 and 3500 pickups because transmission fluid leaks may contact ignition sources, increasing the risk of a fire.

    Product
    RAM — RAM 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V037000·2020-01-23

    Keystone Recalls 2020 Crossroads Trailers Due to Wiring Fire Risk

    Keystone RV is recalling 2020 Crossroads trailers because improper WiFi wiring circuit protection may increase the risk of fire during a short circuit.

    Product
    CROSSROADS — CROSSROADS VOLANTE, HAMPTON, CAMEO, SUNSET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V036000·2020-01-23

    Ram ProMaster Recall: Transmission Shifter Cable May Disconnect

    Chrysler is recalling 2014-2019 Ram ProMaster vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V038000·2020-01-23

    GM Recalls 2014-2015 Cadillac CTS-V Sport for Rear Axle Defect

    General Motors is recalling 2014-2015 Cadillac CTS-V Sport vehicles because rear-axle differential roll pins may fracture, potentially causing the driver to lose control.

    Product
    CADILLAC — CADILLAC CTS-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V040000·2020-01-23

    Rosenbauer Commander Recall: Front Shocks May Separate and Damage Steering

    Rosenbauer America is recalling 2014-2019 Commander vehicles because front shocks may separate, potentially damaging the steering gear and causing a loss of power steering assist.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide