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.

Which agencies issued them

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.

45401–45425 of 76871

  • SevereFDA (Drugs)·D-0681-2017·2017-05-03

    Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 4,001 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2095-2017·2017-05-03

    ConAgra Recalls Premium Hunt's Chili Kits for Potential Salmonella

    ConAgra Foods is recalling Premium Hunt's Chili Kits due to potential Salmonella contamination in the spice packets. The recall covers 5,458 cases distributed nationwide.

    Product
    Premium Hunt's Chili Kit, Total NET WT 44.8 OZ (2.80 LB) 1.27kg; Directions: 1) Cook and stir meat in saucepan over medium-high 7 minutes or until done; drain. 2) Stir in all remaining ingredients; simmer 10 minutes, stirring occasionally. Con Agra Foods, P.O BOX 3768, Dept.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2017·2017-05-03

    Remel Blood Agar Plates Recalled for Listeria Contamination

    Remel Inc is recalling Blood Agar plates due to confirmed surface contamination with Listeria monocytogenes. The products were distributed nationwide and in Puerto Rico.

    Product
    Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1877-2017·2017-05-03

    Cardiovascular Systems Recalls ViperWire Advance Guide Wires Due to Packaging Error

    Cardiovascular Systems Inc is recalling 595 units of ViperWire Advance guide wires because 0.018-inch products were packaged as 0.014-inch.

    Product
    ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14. Product Usage: The Stealth 360 Orbital PAD System and the Diamondback 360 Peripheral Orbital Atherectomy System are percutaneous orbital atherectomy systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1878-2017·2017-05-03

    Ulrich Medical Recalls uNion Cervical Plate System for Screw Mechanism Defect

    Ulrich Medical USA Inc is recalling 4,854 uNion Cervical Plate Systems because static plate screws may disassociate. The recall covers devices distributed in 20 US states.

    Product
    uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the cervical spine (C2 to Ti). The system is to be used to provide stabilization of the anterior cervical spine as an adjunct to fusion for the treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0684-2017·2017-05-03

    Isomeric Pharmacy Recalls Triamcinolone Diacetate Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 1,951 vials of Triamcinolone Diacetate injection because production processes cannot assure sterility. The FDA has classified this as a Class II recall.

    Product
    Triamcinolone Diacetate 40 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1021, barcode 3 70285 10211 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2017·2017-05-03

    Merit Medical Recalls 1 mL Medallion Syringes Due to Plunger Tip Defect

    Merit Medical Systems is voluntarily recalling 1 mL Medallion Syringes because of a defect in the syringe plunger tip.

    Product
    1 mL Medallion¿ Syringe. Catalog Numbers: 701989001, K01-05197P, MSS011-YP, K01-07946P, MSS011, MSS011-LB, MSS011-R, MSS011-Y, MSS011P, MSS011-LBP, MSS011-DG, K08-02926AP, K01-07742P, K10-05457P.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2157-2017·2017-05-03

    Apple Cider Recalled for Elevated Patulin Levels

    Bevovations, LLC is recalling specific apple cider products due to elevated levels of patulin. The recall affects 1,409 cases distributed in New England states.

    Product
    Apple Cider with Potassium Sorbate, 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…
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1884-2017·2017-05-03

    XTANT Medical Recalls 5.5mm CoCr Straight Rods Due to Labeling Error

    XTANT Medical Inc. is recalling 97 units of 5.5mm CoCr Straight Rods because the labels may incorrectly identify the material as Ti6Al-4V ELI instead of Cobalt Chromium.

    Product
    5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one piece per bag. Product Usage: The 5.5mm dia. X 500 mm CoCr Straight Rod is an accessory to the Fortex Pedicle Screw System. It is a straight rod connected…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1875-2017·2017-05-03

    Siemens ACUSON S Family Ultrasound Systems Recalled for Image Display Defects

    Siemens is recalling 2,045 ACUSON S Family ultrasound systems because the 18L6 HD transducer may display a triple image or a dark band, potentially affecting diagnostic accuracy.

    Product
    18L6 HD transducer on the ACUSON S Family ultrasound systems with software versions VD10A or VD10C; Model numbers: 18L6 HD transducer  10041227 & 10789400 S1000  10441701 S2000  10041461 S2000 (Refurb) - 10440017 S3000  10441730 Radiology: The ultrasound imaging…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0678-2017·2017-05-03

    Novartis Recalls Isopto Carpine Eye Drops for Impurity Failures

    Novartis Pharmaceuticals is recalling specific lots of Isopto Carpine eye drops due to failed impurities and degradation specifications.

    Product
    Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4%, packaged in 15 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc. Fort Worth Texas 76134 USA NDC 0998-0206-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1876-2017·2017-05-03

    Becton Dickinson Recalls Trypticase Soy Agar and Chocolate Agar I-Plates

    Becton Dickinson is recalling one lot of Trypticase Soy Agar and Chocolate Agar I-Plates because they may fail to recover specific Haemophilus organisms.

    Product
    BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX)  I Plate Product Usage: Testing - Trypticase Soy Agar with 5% Sheep Blood is used for the growth of fastidious organisms and for the visualization of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V292000·2017-05-02

    Forest River Recalls 2014 XLR Toyhaulers Due to Axle Bolt Issue

    Forest River is recalling 2014 XLR Hyperlite toyhaulers because an axle bolt may not be properly seated, which could cause the axle to shift and lead to a loss of vehicle control.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V299000·2017-05-02

    Prevost Recalls Motor Coaches Due to Trailer Hitch Fastener Loosening Risk

    Prevost is recalling 2014-2017 motor coaches because trailer hitch fasteners may loosen, potentially causing the hitch to detach and increasing crash risk.

    Product
    PREVOST — PREVOST X3-45, H3-45, H3-45 VIP, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17145·2017-05-02

    Goodman Recalls Gas Furnaces Due to Electrical Shock Hazard

    Goodman is recalling about 4,100 gas-fired furnaces because the blower motor is not grounded, posing an electrical shock hazard to individuals servicing the units.

    Product
    Gas-fired furnaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V295000·2017-05-02

    Toyota Recalls 2017 Models for Improper Spare Tire Pressure

    Gulf States Toyota is recalling 2017 models because spare tires were not inflated to the proper pressure, increasing crash risk.

    Product
    TOYOTA — TOYOTA SIENNA, YARIS, RAV4 HYBRID, COROLLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V293000·2017-05-01

    Audi A7 Recall: Head Curtain Air Bags May Not Deploy Properly

    Volkswagen Group of America is recalling 2015-2017 Audi A7 vehicles because head curtain air bags may fail to deploy in a crash, increasing injury risk.

    Product
    AUDI — AUDI A7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V290000·2017-05-01

    Jayco Recalls 2017 Trailers Due to Overheating LED Ceiling Lights

    Jayco is recalling 2017 Jay Flight, Jay Feather, and Hummingbird trailers because LED ceiling lights may overheat, increasing fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FEATHER, JAY FEATHER 7, HUMMINGBIRD, JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V288000·2017-05-01

    Highland Ridge RV Recalls 2017 Models for Overheating LED Ceiling Lights

    Highland Ridge RV is recalling 3,379 2017 fifth wheels and travel trailers because LED ceiling lights may produce excessive heat, increasing the risk of a fire.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ULTRA LITE, OPEN RANGE, LIGHT, ROAMER
    Category
    Vehicle
    Distribution
    Distributed nationwide