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.

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.

57051–57075 of 79657

  • ModerateFDA (Food)·F-2942-2015·2015-08-12

    MedOp Recalls MaxiFlex Multinutrient Formula Due to Out-of-Specification Raw Material

    MedOp Health, Inc. is recalling MaxiFlex Multinutrient Formula dietary supplements because a material review found the Chondroitin Sulfate raw material used was out of specification.

    Product
    ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.
    Category
    Food
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-2349-2015·2015-08-12

    Zimmer Surgical Recalls Tourniquet Cuffs with Missing Instructions

    Zimmer Surgical Inc. is recalling 330 units of 30-inch tourniquet cuffs because the instructions for use were missing usage instructions and warnings.

    Product
    30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder…
    Category
    Medical Device
    Distribution
    45 states
  • ModerateFDA (Drugs)·D-1299-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine and Phentolamine Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling specific vials of Papaverine and Phentolamine Injection because documentation for environmental monitoring during production was missing.

    Product
    SIU-Papav/Phentol 30/.5 mg/mL Injection, Rx Only, 3 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 99999-1775-01
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1315-2015·2015-08-12

    Apothecary Shoppe Recalls Hydroxyprogesterone Caproate Vials for Sterility Concerns

    The Apothecary Shoppe is recalling Hydroxyprogesterone Caproate 250 vials due to lack of documentation for environmental monitoring during production.

    Product
    SIH-Hydroxyprogesterone Caproate 250, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2341-2015·2015-08-12

    Siemens Artis Q Systems Recalled for Potential Liquid Ingress

    Siemens Medical Solutions is recalling Artis Q angiography systems because liquid may seep through the top cover, potentially disabling table movements. No injuries have been reported.

    Product
    Artis Q systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1303-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Tri-Mix Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling SIU-Tri-Mix 18/1/20 Injection because documentation for environmental monitoring during production was missing.

    Product
    SIU-Tri-Mix 18/1/20 Injection, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1563-48
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1291-2015·2015-08-12

    Apothecary Shoppe Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling SIH-Testosterone Cypionate Injection because proper environmental monitoring documentation is missing, raising concerns about sterility.

    Product
    SIH-Testosterone Cyp. 200 mg/mL Injection, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13429-2829-34
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1292-2015·2015-08-12

    Apothecary Shoppe Recalls S-methylcobalamin Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling S-methylcobalamin 25 mg/mL injection vials because documentation for environmental monitoring during production was missing.

    Product
    S-methylcobalamin 25 mg/mL (PF) Injection, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1701-19
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1290-2015·2015-08-12

    Apothecary Shoppe Recalls HCG Injection Due to Sterility Documentation Issues

    The Apothecary Shoppe is recalling HCG 1000 U/mL Injection vials because proper environmental monitoring documentation was missing during production.

    Product
    S-Chorionic Gonad HCG 1000 U/mL Injection, Rx Only, 4 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 14294-1968-80
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1304-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Tri-Mix Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling SIU-Tri-Mix Injection Solution because proper environmental monitoring documentation was missing during production.

    Product
    SIU-Tri-Mix 6/0.33/3.33 Injection Solution, Rx Only, 3 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13429-2007-70
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1307-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Tri-Mix Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling SIU-Tri-Mix 24/1/20 Injection vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.

    Product
    SIU-Tri-Mix 24/1/20 Injection, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1747-39
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2330-2015·2015-08-12

    Roche Cobas b 221 S2 Fluid Pack Recall for Transponder Error

    Roche is recalling S2 Fluid Packs for the Cobas b 221 system because they may generate a transponder error, preventing the instrument from starting measurements.

    Product
    S2 Fluid Pack on the Cobas b 221 system- Catalog Number 03260925184 Blood Gas and Electrolytes Analyzer; The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized…
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-1302-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Tri-Mix Injectable Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 17/0.6/5.7 Injectable in Oklahoma due to lack of assurance of sterility from missing environmental monitoring documentation.

    Product
    SIU-Tri-Mix 17/0.6/5.7 Injectable, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-2348-22
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1298-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine and Phentermine Injection for Sterility Concerns

    The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentermine Injection due to a lack of documentation proving proper environmental monitoring during production.

    Product
    SIU-Papav/Phent 30/1 mg Inj., Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 99999-6830-10
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2339-2015·2015-08-12

    GE Healthcare Recalls MRI Scanners Due to Potential Image Orientation Errors

    GE Healthcare is recalling 82 MRI scanners because a missing spacer may cause images to be flipped left-right with incorrect orientation annotations.

    Product
    GE Healthcare, Signa Infinity MR System; Signa MR/i MR System; SmartSpeed; EchoSpeed Plus; HighSpeed Plus, Signa Infinity MR System with EXCITE Technology, Excite II, Signa 3T Infinity with Excite, Signa Excite 1.5T and Signa Excite 3T, Signa Excite HD, Signa HD 1.5T and Signa…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1310-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Tri-Mix Due to Sterility Documentation Gaps

    The Apothecary Shoppe is recalling SIU-Tri-Mix vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.

    Product
    SIU-Tri-Mix 24 mg/1 mg/10 mcg/mL, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13389-1152-36
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1314-2015·2015-08-12

    Apothecary Shoppe Recalls Phentolamine Vials Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling SIU-Phentolamine 5 mg/mL vials in Oklahoma due to lack of documentation for environmental monitoring during production.

    Product
    SIU-Phentolamine 5 mg/mL in Normal Saline, Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1294-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine Injection Due to Sterility Documentation Gaps

    The Apothecary Shoppe LLC is recalling SIU-Papaverine 30 mg/mL Injection due to a lack of documentation ensuring proper environmental monitoring during production.

    Product
    SIU-Papaverine 30 mg/mL Inj., Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 99999-1775-10
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-1286-2015·2015-08-12

    Perrigo Recalls Subpotent Mometasone Furoate Ointment Tubes Nationwide

    Perrigo Israel Pharmaceuticals is voluntarily recalling 158,268 tubes of Mometasone Furoate Ointment USP, 0.1%, because the product is subpotent.

    Product
    Mometasone Furoate Ointment USP, 0.1%, 15 g tubes, Rx Only, Manufactured by Perrigo, Yeruham 80500, Israel, Distributed by Perrigo, Allegan, MI 49010, NDC 45802-0119-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1285-2015·2015-08-12

    Actavis Recalls Desmopressin Acetate Tablets with Incorrect Imprint

    Actavis is recalling 11,445 bottles of Desmopressin Acetate Tablets because some tablets are incorrectly imprinted with an X.

    Product
    Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA; Distributed by Actavis Pharma, Inc. Parsippany, NJ 07054 USA. NDC: 0591-2464-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2348-2015·2015-08-12

    Zimmer Surgical Recalls Tourniquet Cuffs Due to Missing Instructions

    Zimmer Surgical Inc. is recalling 61 units of 18-inch disposable tourniquet cuffs because the folded instructions for use pamphlet was missing usage instructions and warnings.

    Product
    18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder…
    Category
    Medical Device
    Distribution
    45 states
  • SevereNHTSA·15V505000·2015-08-11

    Mercedes-Benz Recalls 2015-2016 Models for Engine Compartment Fire Risk

    Mercedes-Benz is recalling specific 2015 and 2016 models because a damaged seal may fall into the engine bay, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E400, CLS550, CLS400, E63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V504000·2015-08-11

    Mitsubishi Fuso Trucks Recalled for Brake Pad Shim Corrosion

    Mitsubishi Fuso is recalling certain FEC52, FEC72, and FEC92 trucks because brake pad shims may rust, increasing stopping distance and crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC52, FEC92, FEC72
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V506000·2015-08-11

    Strick Recalls 2013 Dry Freight Van Trailers for Rear Impact Safety Defect

    Strick Trailers is recalling 2013 Dry Freight Van Trailers because the tires are positioned too far forward, failing to meet federal rear impact protection standards.

    Product
    STRICK — STRICK DRY FREIGHT VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide