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.

Which agencies issued them

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.

59651–59675 of 79657

  • ModerateFDA (Devices)·Z-1337-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmet Systems Due to Latex Packaging

    Microtek Medical is recalling 10 Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY, LUMBAR BELT AND MOTOR MODULE, REF 11110STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2015·2015-04-08

    Microtek Smoke Evacuation Tubing Set Recalled for Latex Packaging Labeling Error

    Microtek Medical Inc is recalling 303 Smoke Evacuation Tubing Sets because the packaging contains latex but lacks the required warning label.

    Product
    Smoke Evacuation Tubing Set for Coherent CPG Handpiece, 7/8" x 16' (2.22 cm x 487.88 cm), REF 24244, QTY 3/CS, NON STERILE NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1773-2015·2015-04-08

    Health One Pharmaceuticals Recalls Vigerect Dietary Supplements

    Health One Pharmaceuticals is recalling Vigerect dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Vigerect
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1347-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tube Sets Recalled for Latex Packaging

    Microtek Medical Inc is recalling sterile smoke evacuator tube sets because the packaging contains latex without the required warning label.

    Product
    (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor, Sterile, REF 24155, QTY 10/CS, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1648-2015·2015-04-08

    Health One Pharmaceuticals Recalls Yin Vive Dietary Supplement

    Health One Pharmaceuticals is recalling Yin Vive dietary supplements due to significant violations of cGMP regulations.

    Product
    Yin Vive, 80 Veggie Capsules, 400mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1360-2015·2015-04-08

    Zimmer Recalls Persona Anterior Referencing Sizers Due to Specification Nonconformance

    Zimmer, Inc. is voluntarily recalling 22 lots of Persona Anterior Referencing Sizers with Locking Boom because the devices do not conform to print specifications.

    Product
    Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a sterilizable instrument intended for use in multiple total knee arthroplasty procedures. The Persona Surgical Technique (97-5026-001-00, Rev. 9) states that the sizer…
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Food)·F-1673-2015·2015-04-08

    Health One Pharmaceuticals Recalls Shrink & Clean Dietary Supplement

    Health One Pharmaceuticals is recalling Shrink & Clean dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Shrink & Clean, 60 Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1361-2015·2015-04-08

    King Systems Double Swivel Connector Recalled for Mislabeling

    King Systems Corp. is recalling 900 units of Double Swivel Connectors mislabeled as having a suction port. The error may cause a short procedure delay but poses no risk to patients.

    Product
    Double Swivel Connector with Suction Port Connector, Airway (Extension) King Systems part 7169 Product Usage: An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or gas mask. The double swivel connector with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1343-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tubing Recalled for Unlabeled Latex Packaging

    Microtek Medical is recalling smoke evacuator tubing because the packaging contains latex but lacks the required warning label.

    Product
    TUBING 7/8' X 10', W/WAND & TIP, 24/CS, REF 24187, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1653-2015·2015-04-08

    Health One Recalls True Woman Dietary Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling True Woman dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    True Woman, 60 Vege Capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1679-2015·2015-04-08

    Health One Pharmaceuticals Recalls Griffonia Seed Extract 5-HTP Capsules

    Health One Pharmaceuticals is recalling Griffonia Seed Extract 5-HTP Capsules due to significant violations of cGMP regulations for dietary supplements.

    Product
    Griffonia Seed Extract 5-HTP Capsule, 60 capsules, 100mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1718-2015·2015-04-08

    Health One Pharmaceuticals Recalls Fish Oil 200 for cGMP Violations

    Health One Pharmaceuticals is recalling Fish Oil 200 dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Fish Oil 200
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1744-2015·2015-04-08

    Health One Pharmaceuticals Recalls Passion Secret Dietary Supplements

    Health One Pharmaceuticals is recalling Passion Secret dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Passion Secret
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1671-2015·2015-04-08

    Health One Pharmaceuticals Recalls Four Things Combination Dietary Supplement

    Health One Pharmaceuticals is recalling Four things Combination dietary supplements due to significant violations of current good manufacturing practices (cGMP) regulations.

    Product
    Four things Combination, 100 Vegetarian Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1366-2015·2015-04-08

    Owen Mumford Autoject E1 Fixed Needle Device Recalled for Missing Components

    Owen Mumford USA, Inc. is recalling 3,100 Autoject E1 Fixed needle devices because the syringe carrier is missing a damper and spring.

    Product
    Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.
    Category
    Medical Device
    Distribution
    Distributed nationwide