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.

55301–55325 of 79650

  • HighFDA (Devices)·Z-0276-2016·2015-11-25

    Synthes Sternal ZIPFIX Application Instrument Recall for Screw Failure Risk

    Synthes is recalling 267 previously repaired Sternal ZIPFIX Application Instruments because the screws may break or loosen.

    Product
    Synthes Application Instrument for Sternal ZIPFIX. Indications for use include primary or secondary closure/repair of the sternum following sternotomy or fracture of the sternum to stabilize the sternum and promote fusion.
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-0313-2016·2015-11-25

    Ameditech Recalls Micro Screen 6 Panel Drug Abuse Test Cups

    Ameditech is recalling Micro Screen 6 Panel Cup drug abuse tests because they have shown reduced reactivity.

    Product
    Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0273-2016·2015-11-25

    Philips ECG Sync Cables Recalled for Electrical Interference Risk

    Philips is recalling ECG sync cables used with HeartStart monitors because electrical interference can cause misinterpretation of heart signals or interrupt pacing.

    Product
    ECG Out Cable,for use with a Philips ALS monitor/ defibrillator and bedside monitor for Synchronized cardioversion and Transcutaneous pacing. M1783A/M5526A 12-pin Sync cables, used with HeartStart MRx and HeartStart XL and HeartStart XL+
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0202-2016·2015-11-25

    National Frozen Foods Recalls Italian Blend for Listeria Risk

    National Frozen Foods is recalling Target-exclusive Italian Blend frozen vegetables due to potential Listeria monocytogenes contamination.

    Product
    Italian Blend. Product is IQF frozen, not ready to eat, each label carries cooking instruction. Label reads in part: "*** market pantry *** STEAM-IN-BAG Italian-Style Blend Broccoli, Cauliflower, Carrots, Italian-Style Green Beans & Zucchini*** NET WT 12 OZ***(UPC) 0 85239…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0207-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***MARKON FIRST CROP*** A proof of the label was provided, it does not contain product identity, net wt or ingredients. This product is available in…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V798000·2015-11-25

    Forest River Recalls Motorhomes Due to Unstable Electric Entry Steps

    Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, SPORTSCOACH PATHFINDER, MIRADA, PRISM, PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0206-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling Monarch and Valmont Italian Vegetable Blend due to potential Listeria monocytogenes contamination.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part Item # 58108-03475 "***MONARCH***ITALIAN VEGETABLE BLEND CONTAINS ZUCCHINI, CARROTS, CAULIFLOWER, LIMA BEANS AND ITALIAN GREEN BEANS***NET WT***64…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0272-2016·2015-11-25

    Precision Medical Recalls Easy Dial Oxygen Regulators Due to Label Error

    Precision Medical is recalling 315 Easy Dial Oxygen Regulators because the settings label may be off by one position, causing incorrect oxygen flow.

    Product
    Easy Dial Oxygen Regulator, 168708D and 168715D. Eight liter from .0.25 to 8 liters, 15 liter from 0.5 liter to 15 liters of oxygen per minute.
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Drugs)·D-0349-2016·2015-11-25

    Downing Labs Recalls Taurine Injectable Due to Sterility Concerns

    Downing Labs, LLC is recalling Taurine Injectable, 50mg/mL, 30mL vials due to a lack of assurance of sterility. The recall affects 123 vials distributed nationwide and internationally.

    Product
    Taurine Injectable, 50mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0290-2016·2015-11-25

    Civco Medical Instruments Recalls Large Gauge Infiniti Plus Needle Guides

    Civco Medical Instruments is recalling 54 boxes of Large Gauge Infiniti Plus Needle Guides because the sterility of the product cannot be assured.

    Product
    CIVCO Sales Demo Kit. REF DEMOGPGUIDE Large Gauge Infiniti Plus Needle Guides, used in needle-guided (or catheter) procedures with diagnostic ultrasound transducers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0150-2016·2015-11-25

    Kar's Sweet n' Salty Mix Recalled Due to Possible Glass Contamination

    Kar Nut Products Company is recalling Kar's Sweet n' Salty Mix because the product may contain very small pieces of glass.

    Product
    Kar's Sweet n' Salty Mix Box of 18, 3.5 oz. flexible film bags. 1 box per case.
    Category
    Food
    Distribution
    36 states
  • HighFDA (Food)·F-0208-2016·2015-11-25

    National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk

    National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***GARDEN FRESH***64775***47374***ITALIAN BLEND CONTAINS: ZUCCHINI, CARROTS, CAULIFLOWER, LIMAS, ITALIAN BEANS***20 LB NET WT***" No UPC on blue liner.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0286-2016·2015-11-25

    Civco Infiniti Plus Needle Guide Recalled Due to Sterility Concerns

    Civco Medical Instruments is recalling 717 boxes of Infiniti Plus Needle Guides because the sterility of the product cannot be assured.

    Product
    CIVCO Infiniti Plus Needle Guide, Sterile Needle Guide, 12-18GA, Rx ONLY, STERILE EO. REFs 610-1215, 610-1234, 610-1235, 610-1236. Large Gauge Infiniti Plus Needle Guides, used in needle-guided (or catheter) procedures with diagnostic ultrasound transducers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2016·2015-11-25

    Kar's Sweet n' Salty Mix Recalled for Possible Glass Contamination

    Kar Nut Products Company is recalling 140,322 bags of Kar's Sweet n' Salty Mix due to the possibility that the product may contain very small pieces of glass.

    Product
    Kar's Sweet n' Salty Mix 3.5 oz. flexible film bags. 42 bags per case.
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-0288-2016·2015-11-25

    Civco Biopsy Starter Kit Recalled Due to Sterility Concerns

    Civco Medical Instruments is recalling 1,139 boxes of Biopsy Starter Kits because the sterility of the product cannot be assured.

    Product
    CIVCO Biopsy Starter Kit, Reusable non-sterile bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REFs 10787043, 11001906, 11001906(CMI), 613-247, 613-247(CMI), 620-116, 639-014, 639-016, 639-021, 639-024, 639-025, 639-026, 639-027, 639-033, 639-035, 639-047…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V797000·2015-11-25

    Newmar Recalls 2016 King Aire Vehicles for Missing Emergency Exit Window

    Newmar is recalling 2016 King Aire vehicles that may lack a required emergency exit window over the driver's side dinette table, potentially delaying escape during an emergency.

    Product
    NEWMAR — NEWMAR KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0262-2016·2015-11-25

    US Compounding Recalls Lincomycin/Lidocaine Vials Due to Sterility Concerns

    US Compounding Inc is recalling 1,421 vials of Lincomycin/Lidocaine due to deficient practices that may impact sterility assurance.

    Product
    Lincomycin/Lidocaine (300 mg/1%/mL), 10 mL Multi-Dose Vial, For IV Injection or IV Injection After Dilution, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3104-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0293-2016·2015-11-25

    TZ Medical Neptune Plus Hemostasis Pad Recall for Labeling Mismatch

    TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.

    Product
    Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0232-2016·2015-11-25

    Qualitest Recalls Hydrochlorothiazide Capsules Due to Particulate Matter

    Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.

    Product
    HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0312-2016·2015-11-25

    Ameditech Recalls Immutest Drug Screen Cups Due to Reduced Reactivity

    Ameditech is recalling specific Immutest drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and in Australia.

    Product
    Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5; Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP; Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-12BUP; Immutest 5 panel, Item No. IMCA-5AB-W; Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0298-2016·2015-11-25

    Ameditech Recalls 1 Step 12 Panel Cup Drug Tests

    Ameditech is recalling 787 kits of 1 Step 12 Panel Cup drug tests due to reduced reactivity. The products were distributed in the US and Australia.

    Product
    1 Step 12 Panel Cup, Item No. NBCA-12M-W These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips, including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0311-2016·2015-11-25

    Ameditech Recalls iCup Drug Screen Cups Due to Reduced Reactivity

    Ameditech is recalling iCup drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.

    Product
    iCup Drug Screen Cup, Item No. I-DXA-187-016, I-DXA-167-013; iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142; iCup DX 11 Panel w/Adulterant, Item No. I-DXA-1117-131; iCup DX 12 Panel w/Adulterant, Item No. I-DXA-1127-023; iCup DX 6 Panel w/Adulterant, Item No.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0278-2016·2015-11-25

    Ethicon Harmonic ACE+ 7 Laparoscopic Shears Recalled for Packaging Defect

    Ethicon Endo-Surgery is recalling Harmonic ACE+ 7 Laparoscopic Shears because holes in the Tyvek packaging can compromise the sterile barrier.

    Product
    HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm, 36cm, 45cm length), Ethicon Endo-Surgery. Indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0234-2016·2015-11-25

    Par Pharmaceutical Recalls Meclizine Hydrochloride Tablets Due to Impurity Failures

    Par Pharmaceutical is recalling Meclizine Hydrochloride Tablets because they failed impurity specifications. The recall covers 100 and 1000-count bottles distributed nationwide.

    Product
    Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-035-01) and b) 1000 Ct Bottles (NDC: 49884-035-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.
    Category
    Drug
    Distribution
    Distributed nationwide