The Recall Desk

State

Rhode Island product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34576–34600 of 76791

  • HighFDA (Devices)·Z-1746-2019·2019-06-26

    GE Healthcare Recalls Discovery PET/CT 710 Systems Due to Table Stop Defect

    GE Healthcare is recalling 1,113 Discovery PET/CT 710 systems because the table may stop moving without stopping X-ray exposure.

    Product
    Discovery PET/CT 710 Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1479-2019·2019-06-26

    APS BioGroup Recalls Viralox Oral Spray Due to Bacterial Contamination

    APS BioGroup is recalling Viralox Immune Balancing Polypeptide Oral Spray because testing found elevated levels of Stenotrophomonas maltophilia bacteria.

    Product
    Viralox, UPC 8 63784 00015 0. Immune Balancing Ploypeptide Oral Spray. 5.0 fl. oz. (150 ml) Oral Spray.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1442-2019·2019-06-26

    Zydus Recalls Pramipexole Dihydrochloride Tablets Due to Cross-Contamination

    Zydus Pharmaceuticals is recalling Pramipexole Dihydrochloride Tablets 0.125 mg due to cross-contamination caused by a cleaning failure.

    Product
    Pramipexole Dihydrochloride Tablets 0.125 mg, 1,000-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC 68382-196-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1848-2019·2019-06-26

    Stryker Recalls Endotrac Hook/Triangle Blade Kits Due to Seal Integrity

    Stryker GmbH is recalling 447 Endotrac ECTR Hook/Triangle Blade Kits because the sterile bag seal may be compromised, potentially affecting sterility.

    Product
    Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2056-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1465-2019·2019-06-26

    Macy's Chocolate Pecan Clusters Recalled for Undeclared Allergens

    Gertrude Hawk Brands is recalling R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters because the packaging failed to disclose the presence of almonds and pecans.

    Product
    R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters, 7oz 1 unit per package, oval metal tin canister, 6 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V492000·2019-06-26

    Jerr-Dan Heavy Duty Wrecker Recall for Remote Control Engine Shutdown

    Jerr-Dan is recalling 2018-2019 Heavy Duty Wreckers because the remote control system may cause the engine to shut down unexpectedly, increasing crash risk.

    Product
    JERR-DAN — JERR-DAN HEAVY DUTY WRECKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1745-2019·2019-06-26

    GE Healthcare Recalls Discovery PET/CT 610 Systems Due to X-Ray Safety Issue

    GE Healthcare is recalling 1,113 Discovery PET/CT 610 systems because the table may stop moving while X-ray exposure continues.

    Product
    Discovery PET/CT 610 Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1481-2019·2019-06-26

    APS BioGroup Recalls Immulox Supplement Due to Stenotrophomonas Contamination

    APS BioGroup is recalling Immulox polypeptide supplements due to elevated levels of Stenotrophomonas maltophilia. The recall covers 7,132 units distributed nationwide and in Switzerland.

    Product
    Immulox, UPC 1 82863 000064 6. Immune Balance Polypeptide Supplement with Naturally Occuring Bioactive Peptides. 5.07 oz (150 ml)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1467-2019·2019-06-26

    Gertrude Hawk Almond Toffee Recalled for Undeclared Allergens

    Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Butter Almond Toffee because the packaging failed to disclose the presence of almonds and pecans.

    Product
    R.H. Macy & Co. Milk Chocolate Butter Almond Toffee, 6 oz. 1 unit per package, oval metal tin canister, 6 units per case,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1451-2019·2019-06-26

    Zydus Recalls Methylprednisolone Tablets Due to Cross-Contamination

    Zydus Pharmaceuticals is recalling specific lots of Methylprednisolone tablets due to cross-contamination caused by cleaning failures.

    Product
    METHYLPREDNISOLONE — METHYLPREDNISOLONE (METHYLPREDNISOLONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1842-2019·2019-06-26

    Ethicon Recalls Ethibond Excel Polyester Sutures Due to Endotoxin Risk

    Ethicon, Inc. is recalling specific lots of Ethibond Excel polyester sutures because raw materials used in manufacturing may contain high endotoxin levels.

    Product
    ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX Product Code: X865W Product Usage: ETHIBOND EXCEL Suture is intended for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic and neurological…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1837-2019·2019-06-26

    CIVCO Solstice SRS Immobilization System Recalled for Potential Movement

    Med Tec Inc is recalling 28 units of the CIVCO Solstice SRS Immobilization System because the device may move during patient setup or treatment.

    Product
    CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04 - Product Usage: The Tilting Head Fixation (Solstice) device is comprised of a baseplate and bowl with a locking lever. The bowl is permanently attached to the baseplate and the locking level allows…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1464-2019·2019-06-26

    Macy's Chocolate Pretzels Recalled for Undeclared Almond and Pecan Allergens

    Gertrude Hawk Chocolates is recalling R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzels because the packaging failed to list almonds and pecans.

    Product
    R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzels, 8 oz 1 unit per package, oval metal tin canister, 6 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1839-2019·2019-06-26

    GE Healthcare Recalls Vscan Extend Ultrasound Devices Due to EF Calculation Bias

    GE Healthcare is recalling 119 Vscan Extend ultrasound devices because the LVivo EF app may overestimate ejection fraction values, potentially affecting clinical assessments.

    Product
    LVivo EF app on Vscan Extend. Sold under the following product names: a. Vscan Extend Dual DICOM, Model Numbers H41212ZA, H41212RN; b .Vscan Extend Dual USB, Model Number H41212RK; c. Vscan Extend Dual Wi-Fi, Model Numbers H41212YZ, H41212RL; d. Vscan Extend…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1466-2019·2019-06-26

    R.H. Macy & Co. Dark Chocolate Sea Salt Caramels Recalled for Allergen Mislabeling

    Gertrude Hawk Brands is recalling R.H. Macy & Co. Dark Chocolate Sea Salt Caramels because the packaging failed to disclose the presence of almonds and pecans.

    Product
    R.H. Macy & Co. Dark Chocolate Sea Salt Caramels, 7 oz. 1 unit per package, oval metal tin canister, 6 units per case,
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1799-2019·2019-06-26

    Arrowg+ard Blue Advance JACC Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date listed by Lidstock.

    Product
    Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1788-2019·2019-06-26

    Arrow PICC Kit Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc. is recalling 105 units of Arrow PICC Kits due to incorrect expiration dates on the packaging.

    Product
    Arrow¿ PICC Kit Product Code: ASK 45541 LVH1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1845-2019·2019-06-26

    Zimmer Biomet Recalls Mobi-C Distraction Screws Due to Labeling Error

    Zimmer Biomet is recalling 313 Mobi-C 14mm Distraction Screws because they were incorrectly labeled as 12mm length screws.

    Product
    Mobi-C 14mm Distraction Screw, Quick Start. Intended for cervical intervertebral disc replacement. Item Number: 0024-LDR TEDAN SURGICAL INNOVATIONS LLC DISTRIBUTED BY: LDR SPINE USA, INC., 13785 RESEARCH BLVD, SUITE 200- AUSTIN, TX 78750 Product Usage: The device is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1795-2019·2019-06-26

    Arrow PICC Recall Issued for Incorrect Expiration Date Labeling

    Arrow International Inc is recalling 20 units of Arrow PICC with Chlorag+ard Technology due to an incorrect expiration date on the label.

    Product
    Arrow PICC with Chlorag+ard Technology Product Code: CDA 45541 HPK1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1446-2019·2019-06-26

    Zydus Recalls Pramipexole Dihydrochloride Tablets Due to Cross-Contamination

    Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 0.5 mg due to cross-contamination caused by a cleaning failure.

    Product
    Pramipexole Dihydrochloride Tablets 0.5 mg, 90-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC 68382-198-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1849-2019·2019-06-26

    Stryker Endotrac Hook/Triangle Blade Kit Recall Due to Seal Integrity

    Stryker GmbH is recalling 1,600 Endotrac EPF/EGR Hook/Triangle Blade Kits because the sterile bag seal integrity may be compromised.

    Product
    Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
    Category
    Medical Device
    Distribution
    Distributed nationwide