The Recall Desk

State

Oklahoma product recalls

73,827 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,823
Critical
1,040
Severe
1,494
Most recent
2026-11-04

Of the 5,823 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 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56051–56075 of 79650

  • HighFDA (Devices)·Z-2780-2015·2015-09-30

    Edwards Lifesciences Recalls ThruPort Knot Pusher Due to Suture Fraying Risk

    Edwards Lifesciences is recalling 759 ThruPort Knot Pusher units because the device's tip design may cause suture fraying or splitting, potentially compromising suture knot integrity during cardiac surgery.

    Product
    ThruPort Knot Pusher. This device is sold individually (Model KP1) and as part of the ThruPort Valve Placement Pack (Model VPP). packaged sterile and non-pyrogenic in a sealed, peel-type pouch. The Knot Pusher is a sterile disposable plastic rod used to advance extracorporeal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2811-2015·2015-09-30

    Synthes Cranial Flap Tube Clamp Recalled for Incorrect MR Safe Labeling

    Synthes (USA) Products LLC is recalling Cranial Flap Tube Clamps and Crimping Devices because they were labeled MR Safe without required testing protocols.

    Product
    Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: The Synthes Cranial Flap Tube Clamp System is intended to reattach a cranial bone flap to the surrounding cranium after a craniotomy procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1819-2015·2015-09-30

    Allergan Recalls FML Ophthalmic Ointment Due to Particulate Matter

    Allergan is recalling specific lots of FML ophthalmic ointment because small black particles from the tube cap may be present in the product.

    Product
    FML (fluorometholone ophthalmic ointment) 0.1%, 3.5 g tube, Rx only, Allergan, Inc., Irvine, CA 92612, NDC 0023-0316-04, UPC 3 0023-0316-04 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2807-2015·2015-09-30

    Olympus TJF-Q180V Duodenoscope Recall Issued for Revised Reprocessing Procedures

    Olympus America Inc. is recalling 6,109 TJF-Q180V duodenoscopes to implement new cleaning and disinfection procedures.

    Product
    EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has been designed to be used with an Olympus video system center, light source, documentation equipment, monitors, EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1817-2015·2015-09-30

    Allergan Recalls Refresh Lacri-Lube Eye Ointment Due to Particulate Matter

    Allergan is recalling Refresh Lacri-Lube eye ointment because unscrewing the cap may introduce small black particles into the product.

    Product
    REFRESH LACRI-LUBE — REFRESH LACRI-LUBE (MINERAL OIL, PETROLATUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2805-2015·2015-09-30

    Fujifilm EPX 2500 Operation Manual Recalled for Incorrect Endoscope Specifications

    Fujifilm is recalling 60 EPX 2500 Operation Manuals and sales brochures that incorrectly identify the ED-530XT endoscope's image capabilities.

    Product
    Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1818-2015·2015-09-30

    Allergan Recalls Refresh P.M. Eye Ointment Due to Particulate Matter

    Allergan is recalling Refresh P.M. eye ointment because small black particles from the tube cap may have entered the product.

    Product
    REFRESH P.M. — REFRESH P.M. (MINERAL OIL, PETROLATUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2800-2015·2015-09-30

    Zien Medical PenBlade Safety Scalpel Recalled for Sterile Barrier Risk

    Zien Medical Technologies is recalling PenBlade Safety Scalpels because cracks in the PET trays may compromise the sterile barrier.

    Product
    PenBlade Safety Scalpel, for the incision of human skin and tissue, and to cut or trim sutures and catheters up to 6Fr. Models PB-M-10, PB-M-11P, PB-M-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1820-2015·2015-09-30

    Allergan Recalls Blephamide Ophthalmic Ointment Due to Particulate Matter

    Allergan is recalling 337 tubes of Blephamide ophthalmic ointment because small black particles from the tube cap may be present in the product.

    Product
    BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10 %/0.2 %, 3.5 g tube, Rx only, ALLERGAN, Irvine, California 92612, NDC 0023-0313-04, UPC 3 00230 31304 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2815-2015·2015-09-30

    Siemens RAPIDPoint 500 Lactate Cartridges Recalled for Sodium Bias

    Siemens is recalling 982 RAPIDPoint 500 Lactate cartridges due to a negative sodium bias that affects quality control and patient results.

    Product
    Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part Number: 10491447 Product Usage: The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2806-2015·2015-09-30

    Fujifilm EPX 2500 Processor Manual and Brochure Recall

    Fujifilm is recalling EPX 2500 Processor manuals and brochures that incorrectly identify the ED-530XT endoscope's image quality.

    Product
    Fujifilm Processor EPX 2500 High Definition Endoscopy; (Sales Brochure). For use in endoscopic procedures. Used to observe, record and capture images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2817-2015·2015-09-30

    BD Biosciences Recalls CD4 FITC Reagent Due to Spanish Labeling Error

    Becton, Dickinson and Company is recalling 128 units of CD4 (SK3), FITC reagent because the Spanish text on the label incorrectly identifies the product as CD8 FITC.

    Product
    CD4 (SK3), FITC; Contains CD4 FITC with gelatin and 0.1% sodium Azide. Catalog number 340133 in vitro diagnostic used in Hematology: The SK3 monoclonal antibody reacts with human CD4, a 59-kDa cell surface receptor expressed by a majority of thymocytes, a subpopulation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V608000·2015-09-29

    Ford Recalls 1998-2003 Windstar Minivans for Rear Axle Bracket Defect

    Ford is recalling 1998-2003 Windstar minivans because previously installed rear axle brackets may be misinstalled, potentially allowing the axle to fracture and increasing crash risk.

    Product
    FORD — FORD WINDSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V606000·2015-09-29

    Ford Recalls 2001-2008 Escape and Mariner for Transmission Shift Lever Defect

    Ford is recalling 2001-2008 Escape and Mercury Mariner vehicles with specific remanufactured transmissions because the shift lever bolt may not be tightened, risking vehicle rollaway.

    Product
    FORD — FORD, MERCURY ESCAPE, MARINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V609000·2015-09-29

    GM Recalls 2016 Acadia, Traverse, Enclave for Wiper Motor Fire Risk

    General Motors is recalling 2016 Chevrolet Traverse, GMC Acadia, and Buick Enclave vehicles because the windshield wiper motor may overheat, increasing the risk of a fire.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15255·2015-09-29

    Chewbeads Recalls Pacifier Clips Due to Choking Hazard

    Chewbeads is recalling approximately 45,000 pacifier clips in the U.S. because the D-ring can break, allowing beads to detach and pose a choking hazard.

    Product
    Pacifier clips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15253·2015-09-29

    Bicycles with Front Disc Brakes Recalled for Crash Hazard

    Thirteen manufacturers recall about 1.3 million bicycles with front disc brakes and quick-release levers due to a crash hazard. Consumers should stop using the bikes and contact the manufacturer for a free replacement.

    Product
    Bicycles equipped with front disc brakes and quick release levers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15256·2015-09-29

    Calphalon Recalls Pizza Wheels Due to Handle Detachment and Laceration Risk

    Calphalon is recalling pizza wheels because the handle can detach during use, posing a laceration hazard. Consumers should stop using the product and contact the company for a refund.

    Product
    Pizza wheel pizza cutters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15254·2015-09-29

    Madewell Recalls Katya Sandals Due to Metal Shank Fall Hazard

    Madewell is recalling Katya sandals because a metal shank can dislodge and break through the outsole, posing a fall hazard. No injuries have been reported.

    Product
    Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15257·2015-09-29

    Ross Stores Recalls Rattan Arm Chairs Due to Fall Hazard

    Ross Stores is recalling rattan arm chairs because they may tip or slide backward, posing a fall hazard. Eight reports of minor injuries have been received.

    Product
    Rattan Arm Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V604000·2015-09-28

    Volvo Bus 9700 Recall: Exhaust Clamp Failure May Cause Fire

    Volvo is recalling 2009-2013 9700 buses because a failing exhaust clamp allows hot gas to contact engine materials, increasing fire risk.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V605000·2015-09-28

    Ford Recalls 2015 Taurus, MKS, and 2016 Explorer for Fuel Tank Defect

    Ford is recalling specific 2015 Taurus, Lincoln MKS, and 2016 Explorer vehicles because fuel tank bolts may not be tightened, risking tank separation and fire.

    Product
    FORD — FORD, LINCOLN TAURUS, MKS, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide