The Recall Desk

State

Oklahoma product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52326–52350 of 79647

  • SevereFDA (Drugs)·D-0968-2016·2016-06-15

    Dietary Supplement Recalled for Unapproved Salicylic Acid Content

    Novacare, LLC is recalling Thin and Slim Naturally AM dietary supplements because FDA sampling confirmed the presence of unapproved salicylic acid.

    Product
    Thin and Slim Naturally The Natural Alternative AM Dietary Supplement packaged in 90 capsule containers. Distributed by TSN Labs Inc., P.O. Box 38, Midvale, UT 84047, 1-800-769-7290, www.tsn2000.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V437000·2016-06-15

    Thor Motor Coach Tuscany Recalled for Brake Signal Defect

    Thor Motor Coach is recalling 2014-2016 Tuscany motor homes because the brake signal to towed devices may not deactivate, causing dragging brakes and fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1425-2016·2016-06-15

    Mountain Thins Trail Mix Recalled for Listeria Contamination Risk

    Brown & Haley Inc. is recalling Mountain Thins Trail Mix flavor due to potential Listeria monocytogenes contamination.

    Product
    Mountain Thins Trail Mix flavor, packaged in a stand-up film pouch (resealable), net wt. 5.3 oz. The UPC is 0 41770 33370 7
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1916-2016·2016-06-15

    Hill-Rom Recalls Liko Universal SlingBars Due to Center Bolt Failure Risk

    Hill-Rom is recalling Liko Universal SlingBars because the center bolt may weaken and break, posing a risk of patient falls and injury.

    Product
    Liko Universal SlingBars Universal SlingBar" 350, Universal SlingBar" 350 QRH, Universal SlingBar" 350 R2R, Universal SlingBar" 450, Universal SlingBar" 450 QRH, Universal SlingBar" 450 R2R, Universal SlingBar" 600 Universal SlingBar" 600 QRH Component of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0971-2016·2016-06-15

    FDA Recalls Black Widow 25 Ephedra Fat Burner for Unapproved Ingredient

    Novacare, LLC is recalling Black Widow 25 Ephedra Super Potent Fat Burner because FDA sampling confirmed the presence of salicylic acid in the product.

    Product
    Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0972-2016·2016-06-15

    Methyldrene Original 25 Ephedra ECA Stack Recalled for Unapproved Salicylic Acid

    Novacare, LLC is recalling Methyldrene Original 25 Ephedra ECA Stack dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug.

    Product
    Methyldrene Original 25 Ephedra ECA Stack Extra-Potent Fat Burner Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0961-2016·2016-06-15

    FDA Recalls Fataway Ultimate Stack Supplement for Unapproved Salicylic Acid

    Novacare, LLC is recalling Thin and Slim Fataway Ultimate Stack with Chromium because FDA sampling found unapproved salicylic acid in the dietary supplement.

    Product
    Thin and Slim Fataway Ultimate Stack with Chromium, packaged per 120 capsules. Distributed by Dale H Enterprises Inc. Lewisburg, PA 17837, www.fataway.org.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0969-2016·2016-06-15

    Novacare Recalls Thin and Slim Extreme Stack Fat Burner Supplement

    Novacare, LLC is recalling Thin and Slim Extreme Stack Fat Burner dietary supplements because FDA sampling confirmed the presence of salicylic acid.

    Product
    Thin and Slim Extreme Stack Fat Burner Dietary Supplement packaged in 90 capsule containers. TSN Labs Inc., P.O. Box 38, Midvale, UT 84047, 1-800-769-7290, www.tsn2000.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0973-2016·2016-06-15

    Novacare Recalls Unapproved Dietary Supplements Containing Salicylic Acid

    Novacare, LLC is recalling Xcellerator dietary supplements because FDA sampling confirmed the presence of salicylic acid in products marketed without an approved NDA/ANDA.

    Product
    Xcellerator (product not labeled)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1438-2016·2016-06-15

    Frontier Co-op Hojicha Tea Recalled Due to Potential Salmonella Contamination

    Frontier Natural Products CO-OP is recalling specific lots of Hojicha Tea due to potential Salmonella contamination. Consumers should stop using the affected products.

    Product
    16 oz. foil packages of Frontier Co-op Hojicha Tea Certified Organic Camellia sinensus, Norway, IA 52318
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1922-2016·2016-06-15

    Baxter Recalls Actifuse Bone Void Fillers Due to Endotoxin Concerns

    Baxter Healthcare is voluntarily recalling Actifuse ABX and MIS System bone void fillers because they may contain endotoxin levels above specification criteria.

    Product
    Actifuse ABX/Actifuse MIS System A bone void filler intended only for orthopedic applications as a filler for gaps and voids that are not intrinsic to the stability of the bony structure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1915-2016·2016-06-15

    GE Revolution CT Patient Table Recalled for Unintended Motion Risk

    GE Healthcare is recalling Revolution CT Patient Tables because the cradle can descend on its own, posing a crushing risk to large patients.

    Product
    GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. The system is intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission projection data from the same axial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1714-2016·2016-06-15

    Philips Brilliance iCT CT System Software Defect Recall

    Philips Healthcare is recalling Brilliance iCT Computed Tomography X-Ray Systems due to software defects that cause incorrect scan lengths and dose calculations.

    Product
    Philips Healthcare Brilliance iCT Computed Tomography X-Ray System
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Food)·F-1418-2016·2016-06-15

    Werner Brand Sweet Hot Crunch Mix Recalled for Undeclared Milk Allergen

    Werner Gourmet Meat Snacks is recalling Sweet Hot Crunch Mix because the label declares butter but fails to declare milk, a major allergen.

    Product
    Werner Brand Sweet Hot Crunch Mix, net wt. 2 oz, UPC 7 09972 80120 1. Werner Brand Sweet Hot Crunch Mix, net wt. 6 oz, UPC 7 09972 80100 3. The ingredients statement declared: "***BUTTER TOFFEE PEANUTS (PEANUTS, SUGAR, BUTTER, SALT)***". The label contains…
    Category
    Food
    Distribution
    19 states
  • HighFDA (Devices)·Z-1912-2016·2016-06-15

    DePuy Synthes Flexible Shaft Reamers Recalled for Cytotoxicity Failure

    Synthes (USA) Products LLC is recalling 244 DePuy Synthes 8.0 mm Flexible Shaft Reamers because they failed biological safety evaluations for cytotoxicity.

    Product
    DePuy Synthes 8.0 mm Flexible Shaft Reamer, 360 mm, Orthopedic manual surgical instrument. Part number 351.43
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1917-2016·2016-06-15

    Zimmer Biomet Recalls Persona Trabecular Metal Tibial Plate Instruments

    Zimmer Biomet is recalling specific Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets due to incidents of radiolucent lines and loosening in implants.

    Product
    Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.
    Category
    Medical Device
    Distribution
    30 states
  • HighFDA (Devices)·Z-1925-2016·2016-06-15

    Berchtold Recalls Surgical Table Cushions Due to Potential Staple Contamination

    Berchtold Corp. is recalling 227 HybriGel surgical table cushions because they may contain staples that could appear on patient x-rays.

    Product
    Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional accessory to the Operon Surgical Table. The pads may be attached to the base section with a Velcro fastener. The HybriGel pad shapes and variants can differ depending on the scope of the delivery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1718-2016·2016-06-15

    Philips Healthcare Ingenuity Core128 CT System Software Defect Recall

    Philips Healthcare is recalling 423 Ingenuity Core128 CT systems in the US due to software defects that cause incorrect scan lengths and dose calculations.

    Product
    Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-1937-2016·2016-06-15

    Becton Dickinson Recalls 10 mL Syringes Due to Manufacturing Non-Conformities

    Becton Dickinson is recalling 811,200 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.

    Product
    Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V438000·2016-06-15

    Mercedes-Benz Recalls 2016 C300 Vehicles for Steering Software Error

    Mercedes-Benz is recalling 2016 C300 4Matic vehicles because a software error may cause the electric power steering assist system to shut down, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1936-2016·2016-06-15

    Becton Dickinson Recalls 10 mL Syringes Due to Manufacturing Issues

    Becton Dickinson is recalling 176,000 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.

    Product
    Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1713-2016·2016-06-15

    Philips Brilliance 64 CT System Software Defect Recall

    Philips Healthcare is recalling 423 Brilliance 64 CT systems in the US due to software defects causing incorrect scan lengths and dose calculations.

    Product
    Philips Healthcare Brilliance 64 Computed Tomography X-Ray System
    Category
    Medical Device
    Distribution
    29 states
  • HighNHTSA·16V439000·2016-06-15

    Mercedes-Benz Recalls 2016 SLK and SL Models for Headlight Aim

    Mercedes-Benz is recalling certain 2016 SLK and SL models because low-beam headlights may be aimed incorrectly, potentially reducing driver visibility.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SLK300, SL63, SL550, SLK350
    Category
    Vehicle
    Distribution
    Distributed nationwide