The Recall Desk

State

Oklahoma product recalls

73,824 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,823
Critical
1,040
Severe
1,494
Most recent
2026-11-04

Of the 5,823 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51926–51950 of 79647

  • SevereFDA (Food)·F-1663-2016·2016-07-13

    Pictsweet Steam'ables Summer Vegetables Recalled for Listeria Risk

    The Pictsweet Company is recalling Steam'ables Seasoned Summer Vegetables because they contain onions that may be contaminated with Listeria monocytogenes.

    Product
    PICTSWEET(R) Steam'ables, Seasoned Summer Vegetables, with Cracked Pepper Seasoning, NET WT 10 OZ (283g), UPC 70560 98001, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1659-2016·2016-07-13

    Pictsweet Steamables Spring Vegetables Recalled for Listeria Risk

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

    Product
    PICTSWEET(R) Steamables, Seasoned Spring Vegetables, with Asparagus and Ground Peppercorn Seasoning, NET WT 10 OZ (283g), UPC 70560 97826, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·059-2016·2016-07-13

    Michael Angelo's Recalls Frozen Shrimp Scampi for Undeclared Allergens

    Michael Angelo's Gourmet Foods is recalling frozen shrimp scampi products that may contain undeclared chicken, egg, and soy due to a packaging error.

    Product
    Michael Angelo's Gourmet Foods Inc. — Michael Angelo's Gourmet Foods, Inc. Recalls Shrimp Scampi Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • 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-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 (Devices)·Z-2131-2016·2016-07-13

    GE Healthcare Recalls Discovery MR750w MRI Scanners Due to Burn Risk

    GE Healthcare is recalling 471 Discovery MR750w MRI scanners because a small area of the patient bore can become warm enough to cause a serious burn if proper padding is not used.

    Product
    GE Healthcare, Discovery MR750w
    Category
    Medical Device
    Distribution
    38 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 (Devices)·Z-2133-2016·2016-07-13

    Cadillac First Aid Kit Recalled for Prescription-Only CPR Mask

    Lifeline First Aid LLC is recalling Cadillac First Aid Kits because they contain a CPR mask cleared only for prescription use, not over-the-counter.

    Product
    5195GM, Cadillac First Aid Kit, #23459698, brand General Motors. No UPC.
    Category
    Medical Device
    Distribution
    23 states