The Recall Desk

State

Oklahoma product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47601–47625 of 79640

  • ModerateFDA (Devices)·Z-1529-2017·2017-03-29

    BioMerieux Recalls ETEST Imipenem IP32 Foam Packaging Due to Stability Issues

    BioMerieux SA is recalling ETEST Imipenem IP32 Foam packaging because the current shelf-life claims are not supported by internal testing.

    Product
    ETEST Imipenem IP32 Foam packaging, Product Name: ETEST Imipenem IP 0.002-32. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1484-2017·2017-03-29

    FDA Recalls Microbore Extension Sets Due to Incorrect Priming Volume Labeling

    Vygon MFG is recalling 30,700 AMS-636 Microbore extension sets because the package displays an incorrect priming volume.

    Product
    AMS-636, 60" Microbore extension set. Product Usage: Accessory devices used to administer medical fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1531-2017·2017-03-29

    BioMerieux Recalls ETEST Tobramycin Strips Due to Stability Issues

    BioMerieux SA is recalling ETEST Tobramycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.

    Product
    ETEST Tobramycin TM256 FOAM packaging, Product Name: ETEST Tobramycin TM 0.016-256(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1525-2017·2017-03-29

    BioMerieux Recalls ETEST Vancomycin Strips Due to Stability Issues

    BioMerieux SA is recalling ETEST Vancomycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.

    Product
    ETEST Vancomycin VA 256 FOAM packaging, Product Name: ETEST Vancomycin VA 0.016-256. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1527-2017·2017-03-29

    BioMerieux Recalls Etest Benzyl Penicillin Strips Due to Stability Issues

    BioMerieux SA is recalling Etest Benzyl Penicillin PG256 FOAM packaging because shelf-life claims are not supported by internal testing.

    Product
    ETEST Benzyl Penicillin PG256 FOAM packaging, Product Name: Etest Benzylpenicillin PG 0.016-256 (high). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1524-2017·2017-03-29

    BioMerieux Recalls ETEST Ciprofloxacin CI 32 Foam Due to Stability Issues

    BioMerieux SA is recalling ETEST Ciprofloxacin CI 32 Foam products because their shelf-life claims are not supported by internal testing.

    Product
    Ciprofloxacin CI 32 Foam packaging, Product Name: ETEST Ciprofloxacin CI 0.002-32. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0610-2017·2017-03-29

    AvKARE Recalls Famciclovir Tablets Due to Impurity Levels

    AvKARE Inc. is recalling 116 cartons of 500 mg Famciclovir tablets because the product exceeded specifications for unknown impurities.

    Product
    Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1523-2017·2017-03-29

    BioMerieux Recalls ETEST Ceftriaxone Strips Due to Stability Issues

    BioMerieux SA is recalling ETEST Ceftriaxone antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.

    Product
    ETEST¿ Ceftriaxone TXL32 SPB, Product Name: ETEST¿ Ceftriaxone TX 0.002-32(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1519-2017·2017-03-29

    Teleflex Recalls Non-Latex Nasopharyngeal Airways Due to Labeling Error

    Teleflex Medical is recalling 7,600 units of Green Non-Latex Robertazzi Nasopharyngeal Airways due to a labeling error. The voluntary recall covers products distributed in the US, Canada, and Mexico.

    Product
    Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1518-2017·2017-03-29

    Raindrop Near Vision Inlay Recall for Updated Instructions for Use

    ReVision Optics is recalling 1,279 Raindrop Near Vision Inlays to update instructions for use regarding irrigation and medication timing.

    Product
    Raindrop Near Vision Inlay, Model# RD1-1
    Category
    Medical Device
    Distribution
    29 states
  • LowFDA (Drugs)·D-0609-2017·2017-03-29

    Pfizer Recalls Quillivant XR Methylphenidate Suspension for Dissolution Failure

    Pfizer is recalling specific lots of Quillivant XR extended-release oral suspension because the product failed to meet dissolution specifications at 12 months.

    Product
    Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0608-2017·2017-03-29

    Pfizer Recalls Quillivant XR Methylphenidate Suspension for Dissolution Failure

    Pfizer is recalling Quillivant XR extended-release oral suspension due to failed dissolution specifications at 12 months.

    Product
    Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0607-2017·2017-03-29

    Pfizer Recalls Quillivant XR Methylphenidate Suspension for Dissolution Failure

    Pfizer is recalling Quillivant XR extended-release oral suspension because it failed to meet dissolution specifications at 12 months. The recall affects 28,938 units distributed nationwide.

    Product
    Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V214000·2017-03-28

    Schwarze Street Sweepers Recalled for Air Brake Line Fitting Defect

    Schwarze is recalling 2013-2017 street sweepers because incorrect air brake fittings may cause air leaks and unexpected vehicle stops.

    Product
    SCHWARZE — SCHWARZE A8 TWISTER STREET SWEEPER, M6 AVALANCHE STREET SWEEP, A7 TORNADO STREET SWEEPER, A9 MONSOON STREET SWEEPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17117·2017-03-28

    Look Cycle Recalls Road Bikes and Aerostems Due to Fall Hazards

    Look Cycle is recalling about 800 road bikes and Aerostems because a stainless steel clamp can corrode and break, posing a fall and crash hazard.

    Product
    Look Cycle road bikes and Aerostems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17736·2017-03-28

    SolarWorld Recalls Solar Panel Connectors Due to Electrical Shock Hazard

    SolarWorld is recalling about 97,000 solar panel connectors sold in the U.S. because microscopic cracks can allow moisture to leak in, posing an electrical shock hazard.

    Product
    Connectors sold with solar panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V205000·2017-03-27

    Ford Recalls 2017 Edge Vehicles for Windshield Welding Defect

    Ford is recalling 2017 Edge vehicles with Panoramic Vista Roofs due to an improperly welded windshield header that reduces lateral structural integrity.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V212000·2017-03-27

    Ford Recalls 2017 F-450 and F-550 Superduty Trucks for Driveline Fracture Risk

    Ford is recalling 2017 F-450 and F-550 Superduty trucks because the driveline may vibrate and fracture at highway speeds, potentially causing loss of motive power and increasing crash risk.

    Product
    FORD — FORD F-450 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V211000·2017-03-27

    Great Dane Recalls 2018 Everest SS Trailers Due to Brake Plug Issue

    Great Dane is recalling 2018 Everest SS refrigerated trailers because a front brake chamber plug may be loose, potentially reducing brake pressure and increasing stopping distance.

    Product
    GREAT DANE — GREAT DANE EVEREST SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V209000·2017-03-27

    Ford Recalls 2013-2015 Models Due to Engine Overheating Fire Risk

    Ford is recalling 2013-2015 Escape, Fiesta, Fusion, and Transit Connect vehicles with 1.6L engines because low coolant can cause the engine head to crack, leak oil, and start a fire.

    Product
    FORD — FORD FUSION, ESCAPE, FIESTA, TRANSIT CONNECT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V210000·2017-03-27

    Ford Recalls 2013-2014 Vehicles Due to Door Latch Defect

    Ford is recalling 2013-2014 Lincoln MKZ, Ford Fusion, and 2014 Ford Fiesta vehicles because door latches may break, leaving doors unsecured.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, FIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V206000·2017-03-27

    Keystone Recalls 2017 Cougar Trailers Due to Fire Risk

    Keystone is recalling 2017 Cougar recreational trailers because a manual-resetting circuit breaker near propane storage may spark and cause a fire.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide