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.

58176–58200 of 79657

  • ModerateFDA (Drugs)·D-1139-2015·2015-06-24

    West-Ward Recalls Fentanyl Citrate Injection Due to Impurity Failures

    West-Ward Pharmaceutical Corp. is recalling Fentanyl Citrate Injection due to failed impurities and degradation specifications. The recall covers 14,649 cartons distributed nationwide.

    Product
    FENTANYL CITRATE — FENTANYL CITRATE (FENTANYL CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1800-2015·2015-06-24

    Synthes Recalls 3.7mm Cannulated Screws Due to Incorrect Labeling

    Synthes, Inc. is recalling 54 units of 3.7mm Cannulated Locking and Conical Screws because certain lots were found to have been labeled incorrectly.

    Product
    3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws; . the Cannulated Screws are indicated for fixation of fractures, osteotomies, and non-unions of the clavicle, scapula, olecranon, humerus, radius, ulna, pelvis, tibia, and fibula, particularly in osteopenic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1134-2015·2015-06-24

    Allegiant Health Recalls Famotidine Tablets Due to Manufacturing Investigation Failures

    Allegiant Health is recalling specific lots of over-the-counter famotidine tablets because the manufacturer failed to adequately investigate customer complaints.

    Product
    Famotidine Tablets, USP, 20 mg Tablets, Over the Counter, Made in India and labeled: a) freds Acid Controller, 25 Tablet Cartons, DISTRIBUTED BY: fred's, Inc. 4300 NEW GETWELL RD, MEMPHIS, TN 38118. UPC: 0 84579 12592 0. b) HARMON FACE VALUES MAXIMUM STRENGTH Heartburn RELIEF…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1136-2015·2015-06-24

    Dr. Reddy's Recalls Divalproex Sodium Tablets for Dissolution Failure

    Dr. Reddy's Laboratories is recalling 5,160 bottles of Divalproex Sodium Extended-Release Tablets because they failed to meet dissolution specifications.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1140-2015·2015-06-24

    American Health Packaging Recalls Lamivudine and Zidovudine Tablets for Dissolution Failure

    American Health Packaging is recalling 925 cartons of Lamivudine and Zidovudine Tablets USP 150mg/300mg because they failed dissolution specifications.

    Product
    Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton of 30: NDC 68084-0416-21, Individual dose: NDC 68084-0416-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1135-2015·2015-06-24

    Dr. Reddy's Recalls Divalproex Sodium Tablets for Dissolution Failure

    Dr. Reddy's Laboratories is recalling Divalproex Sodium Extended-Release Tablets because they failed to meet dissolution specifications at the 9-hour time point.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1814-2015·2015-06-24

    CooperSurgical Recalls MILEX OMNIFLEX Diaphragms Due to Packaging Error

    CooperSurgical is recalling 200 units of MILEX OMNIFLEX Diaphragms because size 80 boxes were incorrectly packaged with size 85 diaphragms.

    Product
    MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-1145-2015·2015-06-24

    Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets

    Dr. Reddy's is voluntarily recalling specific lots of Amlodipine and Atorvastatin tablets because they contain less active ingredient than labeled.

    Product
    AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1146-2015·2015-06-24

    Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets

    Dr. Reddy's Laboratories is recalling specific lots of Amlodipine Besylate and Atorvastatin Calcium tablets because they contain less than the labeled amount of active ingredients.

    Product
    AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1143-2015·2015-06-24

    Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets

    Dr. Reddy's is recalling specific lots of Amlodipine and Atorvastatin tablets because they contain less active ingredient than labeled.

    Product
    AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1144-2015·2015-06-24

    Dr. Reddy's Recalls Subpotent Amlodipine and Atorvastatin Tablets

    Dr. Reddy's Laboratories is voluntarily recalling specific lots of Amlodipine Besylate and Atorvastatin Calcium tablets because they contain less than the labeled amount of active ingredients.

    Product
    AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM — AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM (AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1142-2015·2015-06-24

    Ohm Recalls Loratadine Tablets Due to Out-of-Specification Assay

    Ohm Laboratories is recalling Loratadine Orally Disintegrating Tablets because an out-of-specification assay result indicated the drug was superpotent.

    Product
    Loratadine Orally Disintegrating Tablets USP, 10 mg, Antihistamine, Allergy Relief, 24 Hour, 30 Orally Disintegrating Tablets per blister pack, a) Distributed by CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, UPC 050428113677 (CVS brand, b) Distributed by: Walgreen Co.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E053000·2015-06-23

    Suzuki Recalls VZR1800 Accessory Backrest Mounting Hardware Kits

    Suzuki is recalling accessory backrest mounting hardware kits for 2006-2015 VZR1800 motorcycles because incorrect bolts may contact the rear tire, increasing crash risk.

    Product
    SUZUKI — SUZUKI VZR1800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V400000·2015-06-23

    Starcraft RV Recalls 2014-2016 Trailers for Incorrect Tire Certification Labels

    Starcraft RV is recalling 50 model year 2014-2016 AR-ONE and Comet trailers because certification labels list the wrong tire size, which could lead to improper tire installation and increased crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT, STARCRAFT COMET, AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V397000·2015-06-23

    Forest River Recalls 2015 Dynamax Rev for Head Restraint Defect

    Forest River is recalling 2015 Dynamax Rev vehicles because front head restraints may exceed safety limits, increasing injury risk in rear-end collisions.

    Product
    DYNAMAX — DYNAMAX REV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V396000·2015-06-22

    Turtle Top Transit Buses Recalled for Electrical Fire Risk

    Turtle Top is recalling certain 2006-2014 transit buses and specialty vehicles because a loose electrical connection may cause a fire.

    Product
    TURTLE TOP — TURTLE TOP ODYSSEY LT, ODYSSEY, TERRA TRANSPORT, VANTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V393000·2015-06-22

    Jeep Cherokee Recall: Power Liftgate Module Fire Risk

    Chrysler is recalling 2014-2015 Jeep Cherokee vehicles with power liftgates because water intrusion may cause a short circuit and fire.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V389000·2015-06-19

    MCI Motorcoaches Recalled for Hub Carrier Cracking and Oil Leaks

    Motor Coach Industries is recalling certain 2013-2015 D4500, D4505, and J4500 motorcoaches because hub carriers may crack or leak oil, potentially causing loss of vehicle control.

    Product
    MCI — MCI D4505, J4500, D4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15167·2015-06-19

    PetSmart Recalls Top Fin Plastic Aquarium Heaters Due to Electrical Shock Hazard

    PetSmart is recalling Top Fin plastic aquarium heaters due to an electrical problem that poses a risk of fire or electrical shock. Consumers should stop using the heaters and return them for a full refund.

    Product
    Top Fin Plastic Aquarium Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide