The Recall Desk

State

Oklahoma product recalls

20,364 recalls have nationwide distribution and so reach Oklahoma. 0 additional recalls listed Oklahoma specifically in their distribution scope.

About recalls in Oklahoma

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Oklahoma consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

13626–13650 of 20364

  • HighFDA (Devices)·Z-1353-2023·2023-04-19

    PET/CT Imaging System Recall: Software Issue Prevents Image Reconstruction

    Shanghai United Imaging uMI 550 PET/CT imaging system is recalled due to a software defect that may prevent scatter correction during patient scanning, potentially blocking diagnostic PET image generation.

    Product
    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography (PET) and Computed Tomography (CT), Model uMI 550 Part Number: 88000657 88000057
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0722-2023·2023-04-19

    Meal Kits With Animal Crackers Recalled for Metal Shavings

    E S Foods is recalling meal kits nationwide due to potential bronze metal shavings in the animal crackers component. No illnesses have been reported.

    Product
    61119 RS Cinnamon Toast Crunch BB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1350-2023·2023-04-19

    First Response Easy Read App unable to reliably read pregnancy test results

    Church & Dwight's Easy Read App for pregnancy test sticks may fail to display test results or misread them, leading to false positive or false negative results. The app was marketed without required FDA clearance.

    Product
    Easy Read App associated with First Response Pregnancy Test Sticks - Intended use of converting analog pregnancy test results into text pregnant or not pregnant for display on consumer devices (e.g., smart phone, iPad)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1364-2023·2023-04-19

    Inflatable Penile Prosthesis Recalled for Premature Pump Failure Risk

    Coloplast is recalling 13 units of the Titan Touch NB Scrot Zero 18cm inflatable penile prosthesis due to decreased wall thickness that could cause premature pump failure.

    Product
    Titan Touch NB Scrot Zero 18cm, Catalog Number EN29182400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1363-2023·2023-04-19

    Inflatable Penile Prosthesis Risk of Premature Pump Failure

    Coloplast's Titan Touch NB Scrot Zero 16cm prosthesis has been recalled due to decreased wall thickness that could cause premature pump failure. The defect was identified in specific lot units distributed worldwide.

    Product
    Titan Touch NB Scrot Zero 16cm, Catalog Number EN29162400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1360-2023·2023-04-19

    Inflatable Prosthesis Pump Assembly Recalled for Premature Failure Risk

    Coloplast is recalling 9 Titan Pump Assemblies for inflatable penile prostheses due to decreased wall thickness that may cause premature pump failure during normal use.

    Product
    Titan Pump Assembly, Catalog Number 5177701400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1389-2023·2023-04-19

    Chromic Gut Absorbable Sutures recalled due to sterilization failure

    Covidien is recalling Chromic Gut Absorbable Sutures due to a sterilization process failure that may result in unsterile product. Use of affected sutures may cause infection or, in eye surgery, vision loss.

    Product
    Mild Chromic Gut Absorbable Sutures, CH GUT 5-0 12 UD SS-14 SS-14 (G-1766-K), CHROMIC GUT 6-0 45CM HE-1 X12 (G-1780K)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0803-2023·2023-04-19

    Protein bars recalled nationwide for undeclared cashew allergen

    Wellness Natural USA Inc. is recalling SimplyProtein peanut butter chocolate crispy bars sold at Costco due to undeclared cashew allergen. 2.46 million boxes are affected.

    Product
    SimplyProtein¿ Peanut Butter Chocolate Crispy 15-1.41 OZ (40 g) bar. (UPC 6 86207 00914 7) Sold in 15-count variety pack with two other flavors (Lemon Coconut and Chocolate Sea Salt) NET WT 21/16 OZ (600 g). Outside carton UPC 6 86207 80906 8. Packaged in a carboard box. Indiv
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2023·2023-04-19

    BioPlex 2200 Anti-CCP Reagent Kit recalled due to reduced test specificity

    Bio-Rad is recalling BioPlex 2200 Anti-CCP reagent kits due to reduced specificity that may cause false positive results. Four customer complaints documented discrepant results during validation testing.

    Product
    BioPlex 2200, Anti-CCP Calibrator Set, REF 663-3200, IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0707-2023·2023-04-19

    Impossible Chicken Nuggets Recalled for Possible Wood Fragments

    Impossible Foods Inc is recalling 128,029 cases of Impossible Chicken Nuggets nationwide due to possible wood fragments in the product, which pose a choking and injury risk.

    Product
    Impossible Chicken Nuggets Made From Plants, 2x5 lb Bags. Item No. 60-00031. Net Wt.: 10 lb (4.5kg). Not for retail sale. Fully Cooked. Perishable, Keep Frozen. Distributed by: Impossible Foods, Inc., Redwood City, CA 94063.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1388-2023·2023-04-19

    Chromic Gut Absorbable Sutures Recalled for Sterilization Failure Risk

    Covidien, LP is recalling chromic gut absorbable sutures due to sterilization failure that may leave product unsterile, creating risk of infection or vision loss in eye surgery.

    Product
    Chromic Gut Absorbable Sutures, SURGIGUT* 0 CHR GS-25 90CM X36 (CG-904), SURGIGUT* 1 CHR GS-24 90CM X36 (CG-915), CHROMIC GUT 4-0 75CM V20 (GG-121), CHROMIC GUT 3-0 75CM V20 X36 (GG-122), CHROMIC GUT 2-0 75CM V20 X36 (GG-123), CHROMIC GUT 2-0 75CM V26 (GG-127), CHROMIC GUT 4-0 45
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1356-2023·2023-04-19

    X-ray System Models 706100 and 706110 Electrical Fire Risk from Power Surge

    Philips ProxiDiagnost R90 X-ray systems may experience electrical fires if exposed to overvoltage or power surges. The recalled systems affect 243 units distributed nationwide and globally.

    Product
    ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0709-2023·2023-04-19

    Perrona Hot Sauce Recalled Due to Mold Growth on Bottle Exterior

    TIPPCON LLC is recalling Perrona Hot Sauce Original with Chiltepin Peppers due to mold growth on the outside of the bottle. The affected product was distributed nationwide.

    Product
    Perrona Hot Sauce Original with Chiltepin Peppers 5 fl oz (148ml) UPC 75 03016 55507 4 packaged in a PET bottle, 12 bottles per case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0530-2023·2023-04-19

    Pantoprazole Sodium Tablets Recalled for CGMP Deviations and Discoloration

    Hetero USA Inc. is recalling 2,352 bottles of Pantoprazole Sodium 40mg tablets due to manufacturing deviations that caused discoloration. The affected lot (PAN22542, exp. 9/2024) was distributed nationwide.

    Product
    PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0531-2023·2023-04-19

    Bevacizumab Injection Recall Due to Incorrect Lot Number Labeling

    Pine Pharmaceuticals is recalling 932 syringes of Bevacizumab 2.5 mg/0.1 mL due to incorrect lot number labeling on the primary packaging. The affected lot (#66377, expiration 06/28/2023) was distributed nationwide.

    Product
    Bevacizumab 2.5 mg/0.1 mL, Solution for Injection in 1mL, silicone free slip tip syringe, each Syringe supplied in individually labeled poly envelopes (primary packaging). Repackaged by Pine Pharmaceuticals, Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150, Offic
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1374-2023·2023-04-19

    Inflatable Penile Prosthesis Titan Recalled Coloplast Manufacturing Class II

    Coloplast Manufacturing recalls 20 units of Titan 0-Deg Scrotal inflatable penile prosthesis (Lot Numbers 8849601, 8849600, 8849621) with worldwide distribution. The specific reason for the recall is not specified in FDA records.

    Product
    Titan 0-Deg Scrotal 20 Cm, Catalog Number ES89202400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1373-2023·2023-04-19

    Titan Penile Prosthesis Recalled Due to Premature Pump Failure Risk

    Coloplast Manufacturing is recalling the Titan 0-Deg Scrotal 18 Cm inflatable penile prosthesis (25 units) due to decreased wall thickness that may cause premature pump failure. Patients with affected lot numbers should contact their healthcare provider.

    Product
    Titan 0-Deg Scrotal 18 Cm, Catalog Number ES89182400; inflatable penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0529-2023·2023-04-19

    Drug Injection Recall: Norepinephrine Bitartrate Impurity Above Specification

    Sun Pharmaceutical is recalling Norepinephrine Bitartrate Injection due to a chemical impurity exceeding specification limits detected during routine monitoring. The recall affects 16,450 vials distributed nationwide.

    Product
    NOREPINEPHRINE BITARTRATE — NOREPINEPHRINE BITARTRATE (NOREPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1381-2023·2023-04-19

    NanoKnife Surgical Probes Recalled Due to RFID Programming Error

    Angiodynamics recalls NanoKnife 5-Probe Procedure Packs due to a programming error affecting RFID function. The probes may not be recognized by the NanoKnife generator, potentially delaying surgical procedures.

    Product
    NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0532-2023·2023-04-19

    Prescription Drug Recall: Incorrect Expiration Date on MEKTOVI Labels

    Pfizer recalls 1,926 bottles of MEKTOVI (binimetinib) due to incorrect expiration dates on labels. Bottles labeled March 2026 actually expire February 2025.

    Product
    MEKTOVI — MEKTOVI (BINIMETINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0711-2023·2023-04-19

    Perrona Hot Sauce Green Recalled Due to Mold Growth on Bottle Exterior

    TIPPCON LLC is recalling Perrona Hot Sauce Green with Chiltepin Peppers due to mold growth on the outside of the bottle. Approximately 8,230 cases were distributed nationwide.

    Product
    Perrona Hot Sauce Green with Chiltepin Peppers Net 5 FL OZ (148 mL) UPC 7 503016 555098 packaged in a PET bottle, 12 bottles per case
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0535-2023·2023-04-19

    Prescription Epinephrine Kits Recalled for Incorrect NDC Number on Carton

    Focus Health Group is recalling 246 kits of Epinephrine Professional nationwide due to an incorrect NDC number printed on the outer carton. The labeling error does not affect the drug's safety or effectiveness.

    Product
    EPINEPHRINE PROFESSIONAL — EPINEPHRINE PROFESSIONAL (EPINEPHRINE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0710-2023·2023-04-19

    Perrona Hot Sauce Black Recalled Due to Mold Growth

    TIPPCON LLC is recalling Perrona Hot Sauce Black with Chiltepin Peppers due to mold growth detected on the outside of the bottle. No illnesses have been reported.

    Product
    Perrona Hot Sauce Black with Chiltepin Peppers Net 5 FL OZ (148 mL) UPC 75 03016 55511 1 packaged in a PET bottle, 12 bottles per case
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·23177·2023-04-13

    Luxor Audiovisual Carts Recalled for Tip-Over Hazard; Three Deaths Reported

    Luxor Workspaces is recalling approximately 84,700 audiovisual carts that can tip over when loaded with heavy objects like cathode-ray tube televisions. Three children have died and one was seriously injured in tip-over incidents between 2006 and 2016.

    Product
    Luxor A/V carts
    Category
    Consumer Product
    Distribution
    Distributed nationwide