The Recall Desk

State

Oklahoma product recalls

73,738 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,040
Severe
1,493
Most recent
2026-10-28

Of the 5,822 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 1,493 (26%) are Severe.

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35951–35975 of 79560

  • HighNHTSA·19V474000·2019-06-19

    Audi Recalls Vehicles Due to Passenger Air Bag Deactivation Risk

    Audi is recalling specific 2015-2019 models because an electrical issue may cause the passenger air bag to deactivate, increasing injury risk in a crash.

    Product
    AUDI — AUDI A3 CABRIOLET, RS 3, A3 SPORTBACK E-TRON, S3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1399-2019·2019-06-19

    Synthetopes Recalls Pentreotide Vials Due to Lack of Processing Controls

    Synthetopes Inc. is recalling Pentreotide (10 uGm) vials nationwide due to a lack of processing controls. All lots remaining within expiry are affected.

    Product
    Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1342-2019·2019-06-19

    Chiesi Recalls Zileuton Extended-Release Tablets Due to Dissolution Failure

    Chiesi USA is recalling 2,598 bottles of Zileuton Extended-Release Tablets, 600 mg, because they failed dissolution specifications.

    Product
    Zileuton Extended-Release Tablets, 600 mg, 120-count bottles, Rx only, Distributed by: Prasco Laboratories, Mason, OH 45040 USA; NDC 66993-485-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1751-2019·2019-06-19

    GE Healthcare Recalls Prestige Systems Due to Monitor Mount Failure

    GE Healthcare is recalling Prestige II, SI, and VH systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1436-2019·2019-06-19

    Geritrex Recalls Senna Syrup Due to Atypical Odor and Taste

    Geritrex, LLC is recalling 1,536 bottles of Senna Syrup due to reports of atypical odor and unpleasant taste.

    Product
    Senna (sennosides 8.8 mg) Syrup, 8 fl oz. (237 mL) bottles, Rij Pharmaceuticals Corporation 40 Commercial Avenue, Middletown, NY 10941, NDC 53807-556-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1341-2019·2019-06-19

    Chiesi Recalls ZYFLO CR Tablets Due to Dissolution Failure

    Chiesi USA is recalling ZYFLO CR (zileuton) extended-release tablets because they failed to meet dissolution specifications. The recall affects 2,118 bottles distributed nationwide.

    Product
    ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1754-2019·2019-06-19

    GE Healthcare Precision 500D X-ray System Recall for Monitor Mount Failure

    GE Healthcare is recalling Precision 500D X-ray systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1401-2019·2019-06-19

    Synthetopes Recalls Sn-Mertiatide Kit Due to Processing Control Deficiencies

    Synthetopes Inc is recalling Sn-Mertiatide Kits nationwide due to a lack of processing controls. The recall covers all lots remaining within their expiry date.

    Product
    Sn-Mertiatide Kit,1 milligram betiatide, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1767-2019·2019-06-19

    Luminex xTAG Gastrointestinal Pathogen Panel Recalled for Lower MS2 MFI Values

    Luminex Molecular Diagnostics is recalling 965 xTAG Gastrointestinal Pathogen Panel kits due to reports of lower MS2 MFI values.

    Product
    xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple viral, bacterial and parasitic nucleic acids in human stool specimens or human stool (GPP) Kit, IVD, REF I032C0316.
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Drugs)·D-1437-2019·2019-06-19

    Geritrex Recalls Senna Syrup Due to Atypical Odor and Taste

    Geritrex, LLC is recalling Senna Syrup bottles due to reports of atypical odor and unpleasant taste.

    Product
    Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles, Distributed by Geritrex, LLC 40 Commercial Avenue Middletown, NY 10941, NDC 54162-007-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1340-2019·2019-06-19

    Glenmark Recalls Estradiol Vaginal Inserts Due to Defective Plunger

    Glenmark Pharmaceuticals is recalling Estradiol Vaginal Inserts because the plunger delivery system is not functioning properly.

    Product
    ESTRADIOL VAGINAL INSERTS — ESTRADIOL VAGINAL INSERTS (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1773-2019·2019-06-19

    CardioCommand Transesophageal Cardiac Pacing System Recalled for Battery Corrosion

    Cardiocommand Inc. is recalling five units of its Transesophageal Cardiac Pacing and Recording System, Model 7A, due to possible corrosion of the battery contacts.

    Product
    CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left atrial pacing to treat bradycardia, hypotension or AV junctional rhythm - Acceleration of heart rate as an alternative to exercise…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1776-2019·2019-06-19

    Conformis iTotal Hip Replacement System Recalled for Dimensional Discrepancy

    Conformis is recalling 183 iTotal Hip Replacement System stems nationwide due to a 3mm discrepancy between approved and manufactured neck/head lengths.

    Product
    Conformis iTotal Hip Replacement System: HBS-033-00xx-020101, (HIP-PATIENT SPECIFIC STEM RIGHT)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1402-2019·2019-06-19

    Synthetopes Recalls Sulfur Colloid Reaction Vials Due to Processing Controls

    Synthetopes Inc. is recalling Sulfur Colloid Reaction Vials nationwide due to a lack of processing controls.

    Product
    Sulfur Colloid Reaction Vial 1.0 mL, Thaw Before Use, Not for Direct Injection, Store Frozen, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1404-2019·2019-06-19

    Synthetopes Recalls Sn-DTPA Kit Due to Lack of Processing Controls

    Synthetopes Inc is recalling 82 vials of Sn-DTPA Kit 10 mg nationwide due to a lack of processing controls.

    Product
    Sn-DTPA Kit 10 mg, DTPA, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1343-2019·2019-06-19

    B. Braun Recalls Heparin Sodium Bags Due to Low Potency

    B. Braun Medical Inc. is recalling 40,176 bags of Heparin Sodium in Dextrose because testing showed the drug had lower potency than required by USP specifications.

    Product
    HEPARIN SODIUM IN DEXTROSE — HEPARIN SODIUM IN DEXTROSE (HEPARIN SODIUM AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1771-2019·2019-06-19

    Philips Patient Information Center iX Recall for Infusion Pump Data Accuracy

    Philips is recalling Patient Information Center iX software because infusion pump data may be recorded at 100 times the actual rate.

    Product
    Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Information Center iX B.01 (or later); 866390 Patient Information Center iX B.01 upgrade (or later) Product Usage: The intended use of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1400-2019·2019-06-19

    Synthetopes Recalls Sn-DMSA Solution Due to Processing Control Deficiencies

    Synthetopes Inc. is recalling Sn-DMSA solution vials nationwide due to a lack of processing controls. The product is not for direct injection.

    Product
    Sn-DMSA solution, Store Frozen, Not for Direct Injection, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1772-2019·2019-06-19

    Philips IntelliBridge System Recall for Infusion Pump Data Storage Accuracy Issues

    Philips is recalling IntelliBridge Systems configured with comma decimal separators because infusion pump data may be recorded at 100 times the actual values.

    Product
    Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417 IntelliBridge System C.01 (or later) 866418 IntelliBridge System C.01 upgrade (or later) Product Usage: The IntelliBridge System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1406-2019·2019-06-19

    Synthetopes Recalls Sn-Pyrophosphate Kits Due to Processing Control Issues

    Synthetopes Inc. is recalling Sn-Pyrophosphate Kits because of a lack of processing controls. The recall covers all lots remaining within their expiry dates.

    Product
    Sn-Pyrophosphate Kit, 11.9 mg sodium pyrophosphate, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1456-2019·2019-06-19

    Laird Superfood Performance Mushrooms Recalled for Iron Labeling Error

    Laird Superfood is recalling Performance Mushrooms because the label incorrectly lists 14 mg of Iron instead of the actual 14 mcg.

    Product
    Performance Mushrooms product is dried mushroom blend of 4 different mushroom mycelial biomass powders cultured on certified organic oats, brand Laird Superfood, uses as Beverage Booster and Functional Fuel Supplement. Product is packaged in 3.17 oz (90 gram) stand up with…
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1396-2019·2019-06-19

    Bausch & Lomb Recalls Lotemax Ophthalmic Gel for Viscosity Issues

    Bausch & Lomb is recalling Lotemax ophthalmic gel because it failed stability specifications for viscosity. The recall covers 17,083 bottles distributed nationwide.

    Product
    LOTEMAX — LOTEMAX (LOTEPREDNOL ETABONATE)
    Category
    Drug
    Distribution
    Distributed nationwide