The Recall Desk

State

Texas product recalls

73,576 recalls have nationwide distribution and so reach Texas. 12,438 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,438
Critical
1,720
Severe
2,926
Most recent
2026-10-21

Of the 12,438 recalls naming Texas we have scored against our rubric, 1,720 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,926 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28001–28025 of 86014

  • HighFDA (Devices)·Z-1903-2021·2021-06-30

    Blood Culture Identification Panel Recalled Due to Manufacturing Defect

    BioFire BCID2 panels for FilmArray Systems are recalled due to manufacturing defects causing elevated rates of false negative results. Affected diagnostic kits may fail to detect infections in blood culture samples.

    Product
    BioFire BCID2 Panel, REF RFIT-ASY-0147, For FilmArray Systems, CE, Blood Culture Identification Panel in vitro diagnostic, Rx Only, UDI: (01)00815381020338
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1902-2021·2021-06-30

    Ventec VOCSN Ventilators May Shut Down Due to Component Failure

    Ventec VOCSN ventilators may unexpectedly shut down or lose blower function during patient use due to component failure. This could prevent the device from providing ventilation therapy. About 1,934 devices are affected.

    Product
    Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog Number: V+O+C+S+N+Pro/English/PRT-00490-001; V+O+C+S+N+Pro/Japan/PRT-00490-100; V+C+Pro/English/PRT-00900-001; V+C+Pro/Japan/PRT-00900-100; V+C/English/PRT-01098-000…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1938-2021·2021-06-30

    OneTouch Ultra Test Strips Recalled for Potential Inaccurate Glucose Readings

    Cardinal Health Inc. is recalling OneTouch Ultra Test Strips (item 3510443) because temperature excursions during shipping may have compromised glucose measurement accuracy.

    Product
    ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1933-2021·2021-06-30

    Prefilled Pen Needles Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling 1,599 boxes of prefilled pen needles that were exposed to low temperatures during shipping, which may cause inaccurate results. Affected units were distributed in Florida, Georgia, and South Carolina.

    Product
    BD UF PEN 32GX4MM 100 NANO Item Number: 4292272
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0684-2021·2021-06-30

    Clio Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Greek Yogurt Bars (50g x 10 retail packs) distributed nationwide due to the possibility of metal fragments in the product.

    Product
    Clio Greek Yogurt Bar wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC: 867155000206
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1949-2021·2021-06-30

    FDA Recalls Medical Action Minor Procedure Trays for Flaking Metal on Hemostats

    Medical Action Industries is recalling 31 cases of Minor Procedure Trays because hemostats in the kits may have flaking metal or brown spots that could compromise sterile surgical procedures.

    Product
    Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1940-2021·2021-06-30

    OneTouchDelica Lancets Recalled Due to Temperature Exposure During Shipping

    Cardinal Health Inc. is recalling OneTouchDelica Lancets 33G because devices were exposed to freezing temperatures (31.9°F) during shipping, which may cause inaccurate test results.

    Product
    ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0696-2021·2021-06-30

    Clio Strawberry Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Strawberry Greek Yogurt Bars due to the possible presence of metal fragments. The affected product was distributed nationwide.

    Product
    Clio Strawberry Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 861703000113
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0637-2021·2021-06-30

    DermOtic fluocinolone acetonide ear drops recalled for broken glass risk

    Hill Dermaceuticals is recalling DermOtic (fluocinolone acetonide) ear drops due to the potential for broken glass in the glass pipette dropper. The affected product was distributed nationwide.

    Product
    DERMOTIC — DERMOTIC (FLUOCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1929-2021·2021-06-30

    Freestyle Lancets 28G Recalled Due to Temperature Damage During Shipping

    Cardinal Health is recalling Freestyle Lancets due to temperature exposure during shipping that may cause inaccurate results. Affected devices were distributed in Florida, Georgia, and South Carolina.

    Product
    FREESTYLE LANCETS 28G 100CT Item Number:2975670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0683-2021·2021-06-30

    Clio Berry Acai Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Berry Acai flavored Less Sugar Yogurt Bars in Chocolate Coating due to the possible presence of metal fragments. Affected products have best buy dates between April 11, 2021 and June 27, 2021.

    Product
    Clio Berry Acai flavored Less Sugar Yogurt Bar in a Chocolate Coating 45g x 10 Clio Retail 10-pack, UPC: 854021008244
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V493000·2021-06-30

    2021 Porsche Cayenne steering column screw defect may cause loss of control

    Porsche is recalling 2021 Cayenne vehicles because the screw connecting the steering column to the steering box may fail, potentially detaching the steering column and causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0699-2021·2021-06-30

    Good & Gather Sweet Cajun Trail Mix Recalled for Plastic Pieces

    John B. Sanfilippo & Son Inc. is recalling Good & Gather Sweet Cajun Trail Mix because some packages may contain stringy pieces of flexible plastic.

    Product
    Good & Gather Sweet Cajun Trail Mix, Product Number 04659. with Butter Toffee Peanuts, Spicy Seasoned Peanuts, Cajun Sesame Sticks, Roasted Salted Corn Kernels & Honey Roasted Sesame Sticks. Net Wt 11 oz. (311g), UPC 85239-15700
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1947-2021·2021-06-30

    novaplus General Purpose Kit hemostats recalled for potential metal flaking

    Medical Action Industries is recalling novaplus General Purpose Kit (Cat. No. 56603) containing hemostats that may have flaking metal and brown spots on the instruments.

    Product
    novaplus, General Purpose Kit, Cat. No. 56603
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0700-2021·2021-06-30

    Favorite Day Monster Trail Mix Recalled for Plastic Contamination

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Monster Trail Mix (14 oz, Product Number 04313) because the product may contain stringy pieces of flexible plastic. The recall affects approximately 12,017 cases distributed nationwide.

    Product
    favorite day monster Trail Mix, Product Number 04313. Peanuts, M&M'S Milk Chocolate candies, raisins, milk chocolate chips and Peanut Butter Chips. Net Wt 14 oz. (396g), UPC 85239-15675
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0698-2021·2021-06-30

    Clio Vanilla Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla Greek Yogurt Bars (50g x 10 pack, UPC 861703000106) due to the possible presence of metal fragments. The recall affects 196,863 cases distributed nationwide with best-by dates between February 14, 2021 and June 27, 2021.

    Product
    Clio Vanilla Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack. UPC code: 861703000106
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1948-2021·2021-06-30

    Surgical instrument trays recalled for potential flaking metal and brown spots

    Medical Action Industries recalls General Purpose Instrument Trays due to potential flaking metal and brown spots on hemostats. These defects could contaminate surgical instruments.

    Product
    Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0689-2021·2021-06-30

    Clio Expresso Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Expresso Greek Yogurt Bars due to the possible presence of metal fragments. The recall affects 6,733 cases distributed nationwide with best-by dates between February 14, 2021 and July 11, 2021.

    Product
    Clio Expresso Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 867155000244
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1950-2021·2021-06-30

    Econocare Plus Waffle Overlay Recalled for Bodily Fluid Contamination

    EHOB, Inc. is recalling 70 units of the Econocare Plus Waffle Overlay due to trace amounts of dried bodily fluids that may expose patients and healthcare providers to contaminants.

    Product
    Econocare Plus Waffle Overlay- Intended for use as a medical device to aid in the prevention and treatment of pressure injuries or bed sores and general comfort. Product Code: 1025ECP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1941-2021·2021-06-30

    OptiChamber Diamond Spacer Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling 375 OptiChamber Diamond Spacer devices due to temperature exposure during shipping that may cause inaccurate medication delivery results. Affected devices were distributed to Florida, Georgia, and South Carolina.

    Product
    OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0640-2021·2021-06-30

    Metformin Hydrochloride Tablets Recalled for NDMA Contamination

    Viona Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to detection of N-Nitrosodimethylamine (NDMA) levels exceeding acceptable daily intake limits.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1951-2021·2021-06-30

    LEGION Knee Prosthesis Component Recalled for Manufacturing Surface Damage

    Smith & Nephew is recalling 5 units of a knee prosthesis component due to surface damage from a manufacturing error. The affected lot was distributed in specific U.S. states.

    Product
    LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1936-2021·2021-06-30

    OneTouch Ultra Blue test strips recalled for temperature exposure damage

    Cardinal Health is recalling 5,356 boxes of OneTouch Ultra Blue test strips after units were exposed to freezing temperatures during shipping, which may cause inaccurate glucose readings.

    Product
    ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1927-2021·2021-06-30

    Cardiac assessment system may display test reports in wrong patient records

    GE Healthcare's Case Cardiac Assessment System and CardioSoft diagnostic application may display one patient's cardiac test report in another patient's medical record under certain conditions. No patient injuries have been reported.

    Product
    Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0686-2021·2021-06-30

    Clio Vanilla Greek Yogurt Mini Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla Greek Yogurt Mini Bars due to the possibility of metal fragments in the product. Consumers should not consume affected yogurt bars.

    Product
    Clio Vanilla Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008077
    Category
    Food
    Distribution
    Distributed nationwide