The Recall Desk

State

Oklahoma product recalls

73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,824
Critical
1,040
Severe
1,494
Most recent
2026-11-14

Of the 5,824 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 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58376–58400 of 79657

  • HighFDA (Devices)·Z-1704-2015·2015-06-10

    Siemens syngo Workflow SLR Recalled for Potential Order Loss

    Siemens Medical Solutions USA is recalling 131 syngo Workflow SLR systems because a software defect may cause order loss during restarts, leading to diagnosis delays.

    Product
    syngo Workflow SLR; The information system syngo Workflow SLR is a digital radiology information system (RIS) with integrated modules for patient administration, examination, reporting, statistics and system administration. The system electronically displays stores, retrieves…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2355-2015·2015-06-10

    Amy's Enchilada Verde Recalled Due to Listeria Contamination

    Amy's Kitchen is recalling Enchilada Verde products because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.

    Product
    Amy's Enchilada Verde Whole Meal, Spinach and Cheese 10.0 oz (284 g) 12 boxes per case. UPC: 0-42272-00085-2, US distribution only 8 pack, UPC: 0-42272-00085-2 - US Distribution Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2353-2015·2015-06-10

    Amy's Garden Vegetable Lasagna Recalled Due to Listeria Contamination

    Amy's Kitchen is recalling Garden Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used during manufacturing.

    Product
    Amy's Garden Vegetable Lasagna, 10.30 oz (291 g) 12 boxes per case. UPC: 0-42272-00041-8, US distribution only Amy's Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2351-2015·2015-06-10

    Amy's Vegetable Lasagna Recalled Due to Listeria Monocytogenes Contamination

    Amy's Kitchen is recalling Vegetable Lasagna products because supplier-confirmed Listeria Monocytogenes was found in spinach used in manufacturing.

    Product
    Amy's Vegetable Lasagna, 9.5 oz (269 g) 12 boxes per case. UPC 0 42272 00032 6 - US Distribution: UPC 0-42272-90032-9 - Canadian distribution Vegetable Lasagna 8 pack - 9.5 oz, (269g) UPC: 0-42272-00032-6 - US distribution Family Size, 28 oz. (794 g), 8 boxes per case…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2352-2015·2015-06-10

    Amy's Tofu Vegetable Lasagna Recalled Due to Listeria Contamination

    Amy's Kitchen is recalling Tofu Vegetable Lasagna because a supplier notified them that spinach used in the product contained Listeria monocytogenes.

    Product
    Amy's Tofu Vegetable Lasagna, 9.5 oz (269 g) 12 boxes per case. UPC 0-42272-00033-3, US distribution only Amy's Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2363-2015·2015-06-10

    Amy's Gluten Free Vegetable Lasagna Recalled for Listeria Risk

    Amy's Kitchen is recalling Gluten Free Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used in the product.

    Product
    Amy's Gluten Free Vegetable Lasagna, 4.7 oz. 6 boxes per case. Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2359-2015·2015-06-10

    Amy's Gluten Free Tofu Scramble Breakfast Wraps Recalled for Listeria

    Amy's Kitchen is recalling Gluten Free Tofu Scramble Breakfast Wraps because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.

    Product
    Amy's Gluten Free Tofu Scramble Breakfast Wraps, 5.5 oz 156 g) 12 boxes per case. UPC: 0-42272-00807-0, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2361-2015·2015-06-10

    Amy's Brown Rice & Vegetables Bowl Recalled for Listeria Risk

    Amy's Kitchen is recalling Brown Rice & Vegetables Bowls because a supplier notified them that spinach used in manufacturing contained Listeria monocytogenes.

    Product
    Amy's Brown Rice & Vegetables Bowl, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1694-2015·2015-06-10

    Zimmer Recalls 4.5mm Cortical Screws for M/DN Intramedullary Nail System

    Zimmer, Inc. is recalling 4.5mm Cortical Screws for the M/DN system because they are not compatible with the device, potentially causing surgical complications.

    Product
    Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail System, Orthopedic surgical device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1702-2015·2015-06-10

    Alcon Custom Pak Recalled for Potential Glove Splits and Holes

    Alcon Research, Ltd. is recalling Alcon Custom Paks because the Devon Light Glove component may have splits or holes, which could lead to surgical site infections.

    Product
    The Alcon Custom Pak. The Alcon Customer Pak is an assemblage of single-use medical devices and accessories designed by medical professionals for specific ophthalmic surgical procedures. Some Paks contain the Devon Light Glove.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15C002000·2015-06-10

    Baby Jogger Recalls Infant Car Seats Due to Labeling Errors

    Baby Jogger is recalling specific infant car seats because labels and manuals contain incorrect or missing safety information, which may increase injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1113-2015·2015-06-10

    Sucrets Cherry Lozenges Recalled for Incorrect Labeling

    Medtech Products is recalling Sucrets Sore Throat & Cough Vapor Cherry lozenges because an incorrect book label was applied to the tins.

    Product
    SUCRETS Sore Throat & Cough Vapor Cherry lozenges, 18-count tin, Dist. By: Insight Pharmaceuticals, LLC, Trevose, PA 19053-8433
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1700-2015·2015-06-10

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Heparin Activity Failure

    Edwards Lifesciences is recalling 978 Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters because they failed internal statistical tests for heparin activity.

    Product
    Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75. Flow-directed pulmonary artery catheters for monitoring cardiac output, mixed venous oxygen saturation, and end diastolic volume when used with the Vigilance Monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1111-2015·2015-06-10

    Mylan Recalls Mycophenolic Acid Tablets for Dissolution Failures

    Mylan Pharmaceuticals is recalling 7,722 bottles of Mycophenolic Acid Delayed-release Tablets, 180 mg, because they failed to meet dissolution specifications.

    Product
    Mycophenolic Acid Delayed-release Tablets, 180 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A., NDC 0378-4201-78, UPC 3 0378-4201-78 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1708-2015·2015-06-10

    Siemens Dimension Vista LOCI TSH Test Recalled for Inaccurate Results

    Siemens is recalling 2,256 units of the Dimension Vista LOCI TSH test due to a defect that may cause falsely low results.

    Product
    Dimension Vista Systems LOCI Thyroid Stimulating Hormone; the TSH method is an in vitro diagnostic test for the quantitative measurement of Thyroid Stimulating Hormone in human serum and plasma on the Dimension Vista System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1705-2015·2015-06-10

    Siemens Medical Software Recall for Missing Image Measurements on Printouts

    Siemens Medical Solutions is recalling 167 units of Syngo.via and Syngo.x software because measurements on subsequent images do not appear on printouts.

    Product
    Syngo.via and Syngo.x ; a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1112-2015·2015-06-10

    Teva Recalls Zebeta Tablets Due to Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 889 bottles of Zebeta (bisoprolol fumarate) 10mg tablets because they failed dissolution specifications during stability testing.

    Product
    Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1114-2015·2015-06-10

    Fresenius Kabi Recalls KABIVEN IV Bags Due to Amino Acid Labeling Error

    Fresenius Kabi is recalling 5,488 bags of KABIVEN IV solution because the label lists 3.1% amino acids, but the product actually contains 3.3%.

    Product
    KABIVEN — KABIVEN (DEXTROSE, SOYBEAN OIL, ELECTROLYTES, LYSINE, PHENYLALANINE, LEUCINE, VALINE, THREONINE, METHIONINE, ISOLEUCINE, TRYPTOPHAN, ALANINE, ARGININE, GLYCINE, PROLINE, HISTIDINE, GLUTAMIC ACID, SERINE, ASPARTIC ACID AND TYROSINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1115-2015·2015-06-10

    Sandoz Recalls Cetirizine HCl Chewable Tablets Due to Impurity Failure

    Sandoz, Inc. is recalling specific lots of Cetirizine HCl Chewable Tablets because an impurity exceeded specifications during stability testing.

    Product
    Cetirizine HCl Chewable Tablet, 10 mg, 6-tablets in one blister, in 12 (2 blisters) and 24 (4 blisters) tablet count configurations. Manufactured by Sandoz Private Limited Village-Digham Opp. Thane-Belapur Road Navi Mumbai, 400 078, India, for Sandoz Private Limited 100 College…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1707-2015·2015-06-10

    Ortho-Clinical Diagnostics Recalls VITROS Signal Reagent Due to Labeling Defects

    Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products Signal Reagent, Lot 3082, because the reagent packs may contain blank labels.

    Product
    VITROS Immunodiagnostic Products Signal Reagent, Product Code 1072693, Unique Device Identifier No. 10758750008360 VITROS Immunodiagnostics Products Signal Reagent (SR) is supplied to users as a sales unit box containing two Signal Reagent Packs. Each Signal Reagent Pack is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V358000·2015-06-09

    GM Recalls 2015 Cadillac ATS and CTS for Brake Pedal Bracket Fracture

    General Motors is recalling 2015 Cadillac ATS and CTS vehicles because a brake pedal bracket may fracture, preventing the driver from applying the brakes.

    Product
    CADILLAC — CADILLAC CTS, ATS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V359000·2015-06-09

    Forest River Recalls 2016 Trailers Due to Wheel Stud Failure Risk

    Forest River is recalling 1,497 model year 2016 trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER SHOCKWAVE, STEALTH, VIBE, CHEROKEE GREY WOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V357000·2015-06-09

    Kalmar Ottawa T2 Tractors Recalled for Engine Fire Risk

    Kalmar is recalling 2010-2014 Ottawa T2 tractors because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide