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.

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.

54251–54275 of 79650

  • ModerateFDA (Devices)·Z-0772-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Instructions

    Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.

    Product
    IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0774-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMM4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0795-2016·2016-02-17

    PharmaCaribe PulmoSal 7% Sodium Chloride Inhalation Solution Recalled for Mislabeling

    Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).

    Product
    PharmaCaribe PulmoSal 7% Sodium chloride, Inhalation Solution, 7% Sterile, Preservative -free, Non-pyrogenic, pH 7.4 For Inhalation Only Rx Product Usage: The contents of these vials are used in conjunction with a nebulizer for the induction of sputum production where…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0575-2016·2016-02-17

    Bulletproof Recalls Berry FATwater Bottles Due to Microbial Growth

    Bulletproof Digital Inc is recalling 12,583 bottles of Berry FATwater due to microbial growth detection. No pathogens were detected.

    Product
    FATwater bottle, 16.9 fl. oz., Berry flavor, UPC 6 09015 50477 2
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0573-2016·2016-02-17

    Bearded Brothers BOLD Coconut Curry Energy Bars Recalled for Mold

    Bearded Brothers LLC is recalling 128 cases of BOLD Coconut Curry energy bars due to mold. The product was distributed nationwide.

    Product
    Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g UPC: 8-50430-00513-5.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0794-2016·2016-02-17

    Merge Healthcare Recalls RadSuite Picture Archive System for Measurement Errors

    Merge Healthcare is recalling RadSuite picture archive systems because they may display incorrect Standardized Uptake Values (SUV). The recall covers 164 units distributed nationwide.

    Product
    RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344, 5.30.3, 5.30.4, 5.30.4 HF0418E, 5.30.5, 5.30.5 HF0404E, 5.30.5 HF0413E, 5.30.5 HF390E, 5.30.5 SB0368, 5.30.6, 5.30.6 HF0405E, 5.30.6 HF0406E, 5.30.7, 5.30.7…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0780-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMT4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0659-2016·2016-02-17

    Sandoz Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.

    Product
    Candesartan Cilexetil Tablets, 16 mg, a) 30 count (NDC 00781-5938-31) and b) 90 count (NDC 00781-5938-92) bottles, Rx Only, Manufactured by Mylan Laboratories Limited Hyderabad 500 034, India for Sandoz Inc. Princeton, NJ 08540
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0776-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMMB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0577-2016·2016-02-17

    Bulletproof Recalls Tangerine FATwater Bottles Due to Microbial Growth

    Bulletproof Digital Inc is recalling 5,748 bottles of Tangerine FATwater due to microbial growth detection. No pathogens were detected.

    Product
    FATwater bottle, 16.9 fl. oz., Tangerine flavor, UPC 6 41871 93693 9
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0775-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Instructions in Manual

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because critical safety information was missing from the instruction manual.

    Product
    IMPLANT,TM, MTX 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMMB10 Product Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0758-2016·2016-02-17

    Spectranetics Recalls Expired 2.3mm Turbo-Power Laser Atherectomy Catheters

    Spectranetics Corp. is recalling 8 units of 2.3mm Turbo-Power OTW Manual laser atherectomy catheters because they are past their expiration date.

    Product
    2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherectomy Catheter) is a laser atherectomy device designed for use with the CVX-300" Excimer Laser System. The Turbo-Power Laser Atherectomy Catheter is a sterile, single use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0779-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the latest instructions for use.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMT4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0654-2016·2016-02-17

    Fagron Recalls SyrSpend SF Syrup Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF syrup-suspending vehicle due to the presence of yeast. The recall affects 44 bottles distributed nationwide.

    Product
    SyrSpend SF, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 500 mL bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0784-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 16 mm diameter 3.5 mm Catalog #TMTB16 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0660-2016·2016-02-17

    Amerisource Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Amerisource Health Services is recalling 716 cartons of Candesartan Cilexetil Tablets, 16 mg, due to failed impurities and degradation specifications.

    Product
    Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0782-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Instructions in Manual

    Zimmer Dental Inc is recalling specific Trabecular Metal implants because the latest instruction manual omitted critical safety information for certain sizes.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMTB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0777-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Instructions

    Zimmer Dental Inc. is recalling specific dental implants because important safety information was missing from the latest instruction manual.

    Product
    IMPLANT,TM, MTX 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMMB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V086000·2016-02-16

    Starcraft AR-One Toy Hauler Recall for Incorrect Tire Labels

    Starcraft is recalling 2016 AR-One toy hauler trailers because incorrect tire labels may lead to improper tire replacement, increasing crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V087000·2016-02-16

    Mercedes-Benz Recalls 2016 C300 and C450 Models for Sunroof Defect

    Mercedes-Benz is recalling specific 2016 C300 and C450 vehicles because the panoramic sunroof glass may not be properly bonded and could detach during operation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, C450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V088000·2016-02-16

    IMT Recalls Dominator Cranes Due to Valve Bank Cover Defect

    Iowa Mold Tooling is recalling 2013-2016 Dominator vehicles because a valve bank cover may crack and fall off, creating a road hazard.

    Product
    IMT — IMT DOMINATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·016-2016·2016-02-12

    McCain Recalls Bacon Fritters Due To Possible Plastic Contamination

    McCain Foods USA is recalling approximately 25,215 pounds of potato, egg, cheese, and bacon fritters that may contain extraneous plastic materials.

    Product
    McCain Foods USA, Inc. — McCain Foods USA, Inc. Recalls Pork Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·16V085000·2016-02-12

    Trans Tech Student Safety Transporter School Bus Barrier Recall

    Transportation Collaborative is recalling 2012-2015 Trans Tech Student Safety Transporter school buses because the driver's side barrier may not deform properly in a crash.

    Product
    TRANS TECH BUS — TRANS TECH BUS STUDENT SAFETY TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16101·2016-02-12

    Crescent Point Energy Recalls Propane Gas Due to Fire and Burn Hazards

    Crescent Point Energy is recalling approximately 118 million gallons of propane gas in the U.S. because insufficient odorant levels may prevent consumers from detecting leaks, posing fire and burn risks.

    Product
    Propane (LP) Gas
    Category
    Consumer Product
    Distribution
    Distributed nationwide