The Recall Desk

State

Rhode Island product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57201–57225 of 76887

  • SevereFDA (Devices)·Z-1288-2015·2015-03-25

    Ossur LP Rotate Foot System Recalled for Insecure Assembly

    Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.

    Product
    LP Rotate Foot System prosthetic device for fitting lower extremity amputations. -Low profile foot module with adjustable shock absorber and rotation with progressive stiffening -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) with female pyramid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1418-2015·2015-03-25

    Twin City Bagel Recalls Whole Wheat Bagels for Undeclared Peanuts or Almonds

    Twin City Bagel, Inc. is recalling specific brands of whole wheat bagels because they may contain undeclared peanuts or almonds.

    Product
    Whole Wheat bagels sold under the following brands and sizes: 1. Kroger 6 count, UPC 11110-02887 2. Lender's 6 count, UPC 76800-56333 3. L'Oven Fresh Mini 12 count, UPC 41498-17880 4. Pepperidge Farm Mini 17 oz., UPC 14100084938 5. Thomas' 6 count, UPC 4812125505 6.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1276-2015·2015-03-25

    Medtronic FlexCath Select Steerable Sheath Recalled for Valve Debris

    Medtronic is recalling 151 FlexCath Select Steerable Sheaths because clinicians observed debris originating from the hemostasis valve outside of patients' bodies.

    Product
    Medtronic, 10 Fr FlexCath Select Steerable Sheath 990065. The FlexCath Select Steerable Sheath (10 Fr Select) is used for percutaneous catheter introduction into the vasculature and chambers of the heart. The sheath is a single-use device and is not implantable.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1424-2015·2015-03-25

    Kroger Cinnamon Swirl Raisin Bagels Recalled for Undeclared Peanuts or Almonds

    Twin City Bagel, Inc. is recalling Kroger Cinnamon Swirl Raisin Bagels because they may contain undeclared peanuts or almonds.

    Product
    Kroger Cinnamon Swirl Raisin Bagels, 6 count, UPC 11110-02885, and 12 count Mini UPC UPC 11110-02890
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1428-2015·2015-03-25

    Aron Streit Recalls Dark Chocolate Coins for Undeclared Milk

    Aron Streit Inc. is recalling Streit's Kids Dark Chocolate Coins because testing revealed undeclared milk, a major allergen.

    Product
    Streit's Kids Dark CHOCOLATE Coins, 24 x 0.5 oz (15g) mesh bags. UPC 70227 50121. PRODUCT OF TURKEY IMPORTED & DISTRIBUTED BY ARON STREIT INC. NEW YORK, NY 10002 USA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0414-2015·2015-03-25

    Mutual Pharmaceutical Recalls Ergoloid Mesylates Tablets Due to Impurities

    Mutual Pharmaceutical is recalling Ergoloid Mesylates 1 mg tablets because they failed impurity and degradation specifications during stability testing.

    Product
    Ergoloid Mesylates ,1 mg tablets, 100 count bottle, Rx only, Manufactured by MUTUAL PHARMACEUTICAL CO., INC., PHILADELPHIA, PA 19124 USA for Sun Pharmaceutical Industries, Inc. 270 Prospect Plains Road, Cranbury, NJ 08512. NDC 53489-281-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0417-2015·2015-03-25

    Hospira Recalls 5% Dextrose Injection Due to Sterility Concerns

    Hospira is recalling 94,440 bags of 5% Dextrose Injection due to a potential leak at the administrative port that compromises sterility.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·15103·2015-03-25

    Linon Recalls Foldable Wood Patio Chairs Due to Fall Hazard

    Linon Home Décor is recalling about 3,300 foldable wood patio chairs and bistro sets because they can tip over, causing falls.

    Product
    Outdoor Wood Bistro Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1298-2015·2015-03-25

    CooperSurgical Infant Heel Gel Warmers Recalled for Burn Risk

    CooperSurgical is recalling Infant Heel Gel Warmers and The Infant Heel Warmer because products without expiration dates have a remote potential for minor burns.

    Product
    CooperSurgical Infant Heel Gel Warmers, P/N 20418 CooperSurgical The Infant Heal Warmer, P/N 2440 To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2015·2015-03-25

    Stryker Recalls Triathlon Distal Capture Assembly Due to Weld Disassociation Risk

    Stryker Howmedica Osteonics is recalling 2,030 Triathlon Distal Capture Assemblies because a weld may disassociate, potentially causing the trigger mechanism to become loose or disassociated.

    Product
    Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon Distal Capture Assembly is used when a surgeon elects to use a capture for the distal femoral resection or proximal tibial resection in a Triathlon primary total knee arthroplasty (TKA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1238-2015·2015-03-25

    Elekta Precise Treatment Table Recalled for Positioning Error Risk

    Elekta is recalling Precise Treatment Tables because incorrect sensor installation during maintenance can cause undetected positioning errors, potentially leading to clinical mistreatment.

    Product
    Elekta Precise Treatment Table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2015·2015-03-25

    Synthes Thumb Screws Recalled Due to Incorrect Stainless Steel Material

    Synthes, Inc. is recalling 183 thumb screws for orthopedic aiming arms because incorrect raw material was used, which may lead to stress-corrosion cracking.

    Product
    Thumb Screw for the Synthes Recon Locking Aiming Arm for Lateral Entry Femoral Nails-EX (part number 03.010.048) and the Thumb Screw for the Aiming Arm for Titanium Cannulated Tibial Nails-EX (part number 03.010.052). The Recon Locking Aiming Arm for Lateral Entry Femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1300-2015·2015-03-25

    CooperSurgical Recalls MediChoice Infant Heel Warmers for Burn Risk

    CooperSurgical is recalling MediChoice Infant Heel Warmers because products without expiration dates have a remote potential for minor burns.

    Product
    MediChoice WarmGel Infant Heel Warmer, Item # 1643069911 MediChoice Liquid Infant Heel Warmer, Item # 1643069912 Single Use and Disposable. Distributed by: Owens & Minor. To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1450-2015·2015-03-25

    Goya Recalls Kirby Black Beans and Goya Black Bean Soup for Peanut Contamination

    Goya Foods is recalling Kirby Black Beans Creole Seasoning and Goya Black Bean Soup due to possible peanut contamination.

    Product
    Kirby Black Beans Creole Seasoning Net Wt. 29 oz. Packed for Kirby Foods Inc., Miami, Florida 33172 Product of Dominican Republic UPC 0 7738512346 4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes because some packages may have open seals, potentially compromising sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: SafeStep Port Access Kit 22G x 0.75in , SafeStep Port Access Kit 22G x 0.75in with Y-Site, SafeStep Port Access Kit 22G x 1 in , SafeStep Port Access Kit 20G x 0.75in , SafeStep Port Access Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1280-2015·2015-03-25

    Mindray Recalls Passport V Monitors Due to Inaccurate Blood Pressure Readings

    Mindray is recalling 519 Passport V Monitors because the invasive blood pressure function may provide incorrect measurements.

    Product
    Passport V Monitor, Multiparameter Patient Monitor(with Arrhythmia Detection and Alarms) Intended for intra hospital use under the direct supervision of a licensed healthcare practitioner.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1272-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling 16,410 units of BD PosiFlush Saline Flush Syringes included in various device kits because open seals may impact product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerLoc Port Access Kit 19G x 1 in, PowerLoc Port Access Kit 20G x 1 in, , , PowerLoc Port Access Kit 20G x 1.5in, PowerLoc Port Access Kit 20G x 0.75in, , , PowerLoc Port Access Kit 22G x 1 in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1274-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain catheter kits because open seals may compromise product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerGlide Midline Catheter Full Kit (20G) (8cm), PowerGlide Midline Catheter Maximal Barrier Tray (20G) (8cm), PowerGlide Midline Catheter Full Kit (20G) (10cm), The syringe is used to pre-flush…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in various catheter kits because open seals may compromise product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Bard Poly Midline 3F Full Tray (Single-Lumen) (with Microintroducer), Bard Poly Midline 3F Maximal Barrier Tray (Single-Lumen), Bard Poly Midline 4F Maximal Barrier Tray (Single-Lumen) (with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15E024000·2015-03-25

    Gillig Recalls One Recaro Bus Driver Seat Due to Seat Belt Defect

    Gillig is recalling one Recaro bus driver seat because a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2015·2015-03-25

    GE Healthcare Ventilators Recalled for Caster Mounting Hardware Failure Risk

    GE Healthcare is recalling specific ventilator models due to a potential failure of the caster mounting hardware that could cause the device to fall or tip over.

    Product
    GE Healthcare Engstrom Carestation, Engstrom Pro, Cart Only S/5 EC. GE model numbers 1505-8538-000, 1505-9000-000, and 1505-9003-000. Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2015·2015-03-25

    Baxter MiniCap with Povidone-Iodine Solution Recalled for Sponge Defects

    Baxter Healthcare is recalling MiniCap with Povidone-Iodine Solution units for hemodialysis because the product may have separating or protruding sponges.

    Product
    MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1279-2015·2015-03-25

    GE Healthcare Recalls Nuclear Medicine Systems Due to Collimator Detachment Risk

    GE Healthcare is recalling 472 nuclear medicine systems worldwide because a collimator may fall off during rotation. No injuries have been reported.

    Product
    GE Healthcare Millennium VG, Discovery VH and VariCam Nuclear Medicine systems, all configurations. Product Usage: The intended use of the system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1295-2015·2015-03-25

    Transonic Hemodialysis Monitor Recall Due to Inaccurate Flow Measurements

    Transonic Systems Inc is recalling Hemodialysis Monitors that may display zero or low flow values, preventing accurate measurements during dialysis.

    Product
    Transonic Hemodialysis Monitor, Model HD03 -- Product Usage: The Hemodialysis Monitor is intended for use by trained medical personnel to measure delivered blood flow, vascular access recirculation, vascular access blood flow and cardiac output on patients receiving…
    Category
    Medical Device
    Distribution
    Distributed nationwide