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.

49876–49900 of 76871

  • SevereFDA (Food)·F-1653-2016·2016-07-13

    Pictsweet Recalls Frozen Pepper and Onion Blends for Listeria Risk

    The Pictsweet Company is recalling frozen three pepper and onion blends sold under Harris Teeter, Kroger, and Pictsweet brands due to potential Listeria monocytogenes contamination.

    Product
    Frozen three pepper and onion blends labeled as: a) Harris Teeter(TM) brand THREE PEPPER & ONION BLEND, NET WT 12 OZ (340g), UPC 72036 71681, PROUDLY DISTRIBUTED BY HARRIS TEETER, LLC, MATTHEWS, NC 28105 b) Kroger(R) 3 PEPPER & ONION BLEND, onions, green bell peppers…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1662-2016·2016-07-13

    Pictsweet Gumbo Vegetables Recalled for Listeria Risk

    The Pictsweet Company is recalling Pictsweet Gumbo Vegetables because the onions used in the product were recalled for possible Listeria monocytogenes contamination.

    Product
    PICTSWEET(R) Gumbo Vegetables, NET WT 12 OZ (340g), UPC 70560 95995, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1155-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 235 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection, in 2 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock AR --- UPC: 9999993301
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1164-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Midazolam Injection Syringes Nationwide

    Cantrell Drug Company is recalling 1,570 syringes of Midazolam HCl injection because the drug was found to be subpotent. The recall is voluntary and nationwide.

    Product
    MIDAZOLAM HCl in 0.9% Sodium Chloride Injection, 2 mg/2 mL (1 mg/mL), in 2 mL syringe, Rx only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-001-16 UPC: 0100352533001161
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1153-2016·2016-07-13

    Cantrell Recalls Subpotent Atropine Sulfate Injection Syringes Nationwide

    Cantrell Drug Company is recalling specific lots of Atropine Sulfate Injection Solution because the drug was found to be subpotent.

    Product
    Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL), in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1613-2016·2016-07-13

    Sid Wainer Tart Shells Recalled for Undeclared Egg Allergen

    Sid Wainer and Son is recalling Domaine de Provence La Cucina Tart Shells because the product contains undeclared eggs, a major food allergen.

    Product
    Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son, New Bedford, MA UPC Code: 708152149119 Item Number: 149110
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-1658-2016·2016-07-13

    Kroger Stir Fry Starters Recalled for Possible Listeria Contamination

    The Pictsweet Company is recalling Kroger Stir Fry Starters because the onions included may be contaminated with Listeria monocytogenes.

    Product
    Kroger(R) VEGETABLES, broccoli, sugar snap peas, green bean carrots, celery, onions, mushrooms, & red bell peppers, STIR FRY STARTERS(R), NET WT 12 OZ (340g), UPC 11110 89775, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1664-2016·2016-07-13

    Pictsweet Deluxe Stir-Fry Vegetables Recalled for Listeria Risk

    The Pictsweet Company is recalling Deluxe Stir-Fry Chinese Style Vegetables because they contain onions that may be contaminated with Listeria monocytogenes.

    Product
    PICTSWEET(R) Deluxe Stir-Fry Chinese Style Vegetables, Oriental Seasoning, NET WT 24 OZ (1 LB 8 OZ) 680g, UPC 70560 95689, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1161-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Lidocaine HCl Injection Syringes

    Cantrell Drug Company is recalling 450 syringes of Lidocaine HCl 1% injection due to subpotent drug levels. The recall is voluntary and nationwide.

    Product
    LIDocaine HCl 1% BUFFERED WITH SODIUM BICARBONATE Injection, packaged in 3 mL Syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992033
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1614-2016·2016-07-13

    Sid Wainer & Son Recalls Tart Shells for Undeclared Coconut Allergen

    Sid Wainer & Son is recalling Domaine de Provence Neutral 3" Cone Tart Shells because they contain undeclared coconut, a major food allergen.

    Product
    Domaine de Provence Neutral 3"¿ Cone Tart Shells Produced Exclusively for Sid Wainer & Son, New Bedford, MA UPC Code: 708152316856 Item Number: 316850
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-2129-2016·2016-07-13

    Medtronic PoleStar MRI System Components Recalled for Electrical Shock Risk

    Medtronic Navigation is recalling PoleStar MRI system components due to misplaced ground pins that may cause electrical shock to users.

    Product
    PoleStar system (N20 / N30) Warning Lamps Control Box, Warning Lamps Control Box Cables, Thermoflex Chiller Product The PoleStar Surgical MRI System is intended for use as an intraoperative imaging device to produce MRI images of sections of the head selected by the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2082-2016·2016-07-13

    Medtronic 0-arm Imaging mobile x-ray system recall for battery damage risk

    Medtronic is recalling 0-arm Imaging mobile x-ray systems because replacement batteries may be damaged during shipment, creating a risk of failure.

    Product
    Medtronic 0-arm Imaging mobile x-ray system. Model Numbers - B1-700-00027, B1-700-00028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2016·2016-07-13

    Toshiba Vantage Titan 3T MRI System Recalled for Gradient Coil Issue

    Toshiba American Medical Systems is recalling 33 Vantage Titan 3T MRI systems due to a potential problem with the gradient coil.

    Product
    MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product Usage: Vantage Titan 3T (MRT-3010, M-Power V3.5) is an open-bore 3T MRI system that permits outstanding image quality without compromising on features or performance. Vantage Titan 3T combines the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2130-2016·2016-07-13

    Custom Ultrasonics System 83 Plus Endoscope Washer Recall Issued

    Custom Ultrasonics is recalling System 83 Plus endoscope washer/disinfectors to warn customers not to use them for duodenoscopes until further notice.

    Product
    The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible submersible endoscopes that are used in the gastrointestinal and/or pulmonary tracts.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1160-2016·2016-07-13

    Cantrell Drug Recalls Heparin Sodium Syringes Due to Stability Data Concerns

    Cantrell Drug Company is recalling 4,170 syringes of Heparin Sodium in 0.45% Sodium Chloride because stability data does not support the expiration date.

    Product
    HEPARIN Sodium in 0.45% Sodium Chloride, 1 USP Unit/2 mL (0.5 USP Units/mL), Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-148-16, UPC: 0100352533148163
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1063-2016·2016-07-13

    Dr. Reddy's Recalls Sirolimus Tablets Due to Impurity

    Dr. Reddy's Laboratories is recalling specific lots of Sirolimus tablets because they failed impurity specifications for secorapamycin.

    Product
    SIROLIMUS — SIROLIMUS (SIROLIMUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1617-2016·2016-07-13

    Zarbee's Baby Omega 3 Liquid Supplement Recalled for Contaminants

    Zarbee's Naturals is recalling Baby Omega 3 liquid supplements because some units contain elevated aerobic plate counts and do not meet visual appearance standards.

    Product
    Baby Omega 3 Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1159-2016·2016-07-13

    Cantrell Drug Recalls Heparin Sodium Syringes Due to Stability Data Issues

    Cantrell Drug Company is recalling 352 syringes of Heparin Sodium 0.5 USP UNITS/mL because stability data does not support the expiration date.

    Product
    HEParin Sodium 0.5 USP UNITS/mL in 0.225% SODIUM CHLORIDE, in 3 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992212
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2136-2016·2016-07-13

    Arrow Recalls Central Venous Catheters Due to Length Mismatch

    Arrow International Inc. is recalling specific lots of central venous catheters because kits labeled for 20 cm catheters may contain 16 cm catheters.

    Product
    ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER. Product Usage: Indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring cental venous access including, but not limited to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1163-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Midazolam Syringes Nationwide

    Cantrell Drug Company is recalling 212 syringes of Midazolam HCl that may contain less than the labeled amount of active ingredient.

    Product
    MIDAZolam HCl 0.1 mg/mL in 5% DEXTROSE 2.5 mL syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999993721
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2004-2016·2016-07-13

    Musculoskeletal Transplant Foundation Recalls AFT Diverted Tubes Due to Unsealed Pouch

    Musculoskeletal Transplant Foundation is recalling 114 AFT Diverted Tubes because an unsealed Tyvek pouch could introduce contamination into the sterile field.

    Product
    Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine. Product Code: 227005.
    Category
    Medical Device
    Distribution
    Distributed nationwide