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.

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.

47951–47975 of 79640

  • SevereNHTSA·17V131000·2017-03-01

    REV Recalls 2017 Ambulances Due to Rear Brake Bolt Torque Issue

    REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.

    Product
    MARQUE — MARQUE, FRONTLINE, WHEELED COACH TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1165-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Trial Trays Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System trial trays due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1498-2017·2017-03-01

    Palmer's Candies Creme De Menthe Bark Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Creme De Menthe Bark because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Creme De Menthe Bark, A) NET WT 9 OZ (255 g) packaged in cardboard boxes, UPC Code 77232-16043, B) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPS code 77232-17255; C) NET WT 10 lbs Net Weight (4.54 kg) packaged in cardboard boxes
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1502-2017·2017-03-01

    Palmer's Candies Peppermint Bark Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling Peppermint Bark candy because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPC Code 77232-17270; B) NET WT 10 OZ (283 g) packaged in paper bags, UPC 77232-23091; C) NET WT 8 OZ (226 g) packaged in paper boxes UPC 77232-12146; C) NET WT 9 OZ (255 g)…
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1505-2017·2017-03-01

    Palmer Candy Recalls Trail's End Chocolatey Crunch Due to Salmonella Risk

    Palmer Candy Co is recalling Trail's End Gourmet Chocolatey Crunch because an ingredient may be contaminated with Salmonella.

    Product
    Trail's End Gourmet Chocolatey Crunch A) NET WT 18 OZ (1.13 LB) 510 g, packaged in foil bags; B) NET WT 15 OZ packaged in foil bags;
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·F-1510-2017·2017-03-01

    Palmer's Chocolatey Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling 198 cases of Palmer's Candies Chocolatey Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10798
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-1167-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Devices)·Z-1164-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Drugs)·D-0480-2017·2017-03-01

    Hospira Recalls Metronidazole Injection Bags Due to Leaking

    Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.

    Product
    METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1161-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1172-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Material Inclusions

    Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1225-2017·2017-03-01

    Tosoh HLC-723G8 Analyzer Recalled for HbA1c Test Inaccuracy

    Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.

    Product
    Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-1174-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1157-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1228-2017·2017-03-01

    Arrow International Recalls Vascular Catheter Introduction Kits Due to Flaring Sheaths

    Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.

    Product
    Vascular catheter introduction kit The PICC is indicated for short or long term peripheral access to the central Venous system for intravenous therapy, blood sampling, infusion and power injection of contrast media.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1152-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.

    Product
    Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1173-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1159-2017·2017-03-01

    Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-1527-2017·2017-03-01

    Falafel King Recalls Tzatziki Sauce for Undeclared Milk Allergen

    Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.

    Product
    Falafel King Tzatziki Sauce. 10 ounce. Plastic container
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1170-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1158-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·17V127000·2017-03-01

    Volvo Recalls 2017 Models for Side Air Bag Inflator Defect

    Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.

    Product
    VOLVO — VOLVO V60, XC60, S60, V60CC
    Category
    Vehicle
    Distribution
    Distributed nationwide