The Recall Desk

State

Texas product recalls

73,366 recalls have nationwide distribution and so reach Texas. 12,434 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,434
Critical
1,720
Severe
2,926
Most recent
2026-10-07

Of the 12,434 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 12,434 recalls whose distribution notice names Texas specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19626–19650 of 85800

  • HighFDA (Devices)·Z-1089-2023·2023-02-15

    Sterile surgical trays recalled due to packaging puncture risk

    MEDLINE INDUSTRIES is recalling six models of sterile surgical trays due to a potential for blades within the kits to puncture the sterile packaging. Affected trays were distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. GYN LAPAROTOMY HARPER PACK-LF b. OB GYN LAP PACK-LF c. VAGINAL HYSTERECTOMY PACK d. DELTA PACK e. MAJOR VAGINAL-LF f. GYN LAPAROSCOPY II
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1092-2023·2023-02-15

    Sterile Procedural Trays With Blades That May Puncture Packaging

    Medline recalls sterile surgical trays because internal blades can puncture the outer protective foil packaging, potentially compromising sterility.

    Product
    Sterile Procedural Trays, labeled as the following: a. C-SECTION OR 30 CDS b. C-SECTION CDS c. C-SECTION CDS d. C-SECTION CDS e. MAJOR ORTHO CDS-LF f. C-SECTION CDS g. C-SECTION CDS h. C-SECTION PROCEDURE i. C-SECTION CDS-LF j. C-SECTION CDS k. C-SECTION CDS l.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1067-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Puncture Risk

    Medline Industries is recalling sterile procedural trays because sterile blades within the kits may puncture the protective foil packaging. Approximately 12,964 cases (23,379 units) distributed worldwide are affected.

    Product
    Sterile Procedural Trays, labeled as the following: a. EP LAB PACEMAKER PACK b. OPEN HEART CDS c. OPEN HEART CDS d. AAA CDS e. OPEN HEART CDS f. PACEMAKER CDS g. HEART CDS h. VALVE PACK i. OPEN HEART CDS-3 j. OPEN HEART PACK k. OPEN HEART PACK l. OPEN HEART ADULT m. OPEN HEART…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1073-2023·2023-02-15

    Sterile Procedural Trays Recalled for Potential Blade Puncture

    Medline sterile procedural trays for minor and breast biopsies are being recalled because sterile blades may puncture the outer foil packaging, compromising sterility. The recall affects 237 cases (1,242 units) distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. MINOR/BREAST BIOPSY-LF b. BREAST BIOPSY-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1083-2023·2023-02-15

    Medline Sterile Procedural Trays Recalled for Potential Blade Puncture in Packaging

    Medline Industries is recalling sterile procedural trays because blades in the kits may puncture the outer foil sterile packaging, compromising sterility. No injuries have been reported.

    Product
    Sterile Procedural Trays, labeled as the following: a. MAJOR CDS-LF b. BURN PACK-LF c. BURN PACK d. SMALL BURN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1062-2023·2023-02-15

    Medline sterile procedural trays recalled for blade packaging puncture

    Medline is recalling sterile procedural trays (Lot 22IBG550) because sterile blades can puncture the foil packaging, compromising sterility. Units were distributed worldwide.

    Product
    LOCAL PACK. Sterile Procedural Tray.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1099-2023·2023-02-15

    Spinal Cement System Recalled for Incorrect Expiration Date

    TEKNIMED SAS is recalling HIGH V+ Spinal Cement System (236 units) due to mislabeling showing expiration date of February 28, 2027 instead of the correct date February 28, 2025.

    Product
    HIGH V+ Spinal Cement System REF T040321K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1064-2023·2023-02-15

    Sterile Procedural Trays Recalled Over Potential Blade Puncture of Packaging

    Medline Industries is recalling sterile procedural trays because sterile blades inside could puncture the outer foil packaging, compromising sterility. The recall affects units distributed worldwide.

    Product
    UNIVERSAL CORE DR RUNNELS PACK. Sterile Procedural Tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1098-2023·2023-02-15

    Zimmer Identity Shoulder Resection Planer Units Recalled for Malfunction

    Zimmer, Inc. is recalling 84 units of the Identity Shoulder System Resection Planer due to defects discovered during training testing. Some units are unusable, potentially affecting surgical performance in shoulder procedures.

    Product
    Identity Shoulder System Resection Planer 35mm Resection Planer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1104-2023·2023-02-15

    Roche cobas Flu/COVID assay recalled for false negative influenza results

    Roche Molecular Systems recalls cobas SARS-CoV-2 & Influenza A/B assay kits used in clinical laboratories. The kits may produce false negative Influenza A results, potentially delaying accurate diagnosis.

    Product
    cobas SARS-CoV-2 & Influenza A/B Qualitative assay for use on the cobas 6800/8800 Systems; Material number 09233474190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V082000·2023-02-15

    Travel trailers recalled for fuel station controller fire risk

    Keystone RV is recalling certain 2021-2023 travel trailers because the fuel station controller may fail, increasing fire risk. Free repairs are available through dealers.

    Product
    KEYSTONE — KEYSTONE FUZION, IMPACT, RAPTOR, CARBON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Puncture Risk

    Medline Industries is recalling sterile procedural trays (ENDOSCOPY-LF and SEPTO/ENDO) because sterile blades may puncture the outer foil layer of the sterile packaging. The recall affects units distributed nationwide and internationally.

    Product
    Sterile Procedural Trays, labeled as the following: a. ENDOSCOPY-LF b. SEPTO/ENDO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1052-2023·2023-02-15

    NuVasive Pulse III Multimodality System remote monitoring connection failure

    An incorrect security key prevents the NuVasive Pulse III system from connecting to remote monitoring during spinal, thoracic, and extremity surgeries. Affected facilities should contact NuVasive for corrective action.

    Product
    NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0265-2023·2023-02-15

    Akorn Atropine Sulfate Eye Solution Recalled for Failed Stability Testing

    Akorn is recalling 45,117 bottles of Atropine Sulfate Ophthalmic Solution because stability testing found viscosity measurements out of specification. The affected product should not be used.

    Product
    Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V079000·2023-02-14

    2022-2023 BMW IX and X1 driver airbag may fail to deploy in crash

    Certain 2022 and 2023 BMW IX and X1 vehicles have defective driver-side airbags that may not deploy during a crash. Dealers will replace the airbags at no charge.

    Product
    BMW — BMW X1, IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V080000·2023-02-14

    2019-2022 Subaru Crosstrek Hybrid battery charging system recall

    Subaru is recalling 2019-2022 Crosstrek Hybrid vehicles because the harness terminal supplying power to the 12-Volt battery may corrode and break, preventing charging. A non-functioning battery can cause loss of drive power and increase crash risk.

    Product
    SUBARU — SUBARU CROSSTREK HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E014000·2023-02-13

    Braun Recalls Child Seat Weldments Due to Improper Welds

    Braun Corporation is recalling child seat weldments for the BraunAbility Turny Seat because improper welds may cause anchors to detach in a crash.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V076000·2023-02-13

    Subaru Recalls 2004-2005 Impreza and WRX for Air Bag Defect

    Subaru is recalling 2004-2005 Impreza and WRX vehicles because previously replaced passenger air bag inflators may have been installed incorrectly, increasing injury risk in a crash.

    Product
    SUBARU — SUBARU IMPREZA, WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V078000·2023-02-13

    Proterra Catalyst and ZX5 buses recalled for wiper motor failure

    Proterra is recalling certain 2020–2022 Catalyst and ZX5 buses due to windshield wiper motor failure. Inoperative wipers reduce visibility and increase crash risk.

    Product
    PROTERRA — PROTERRA CATALYST, ZX5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V074000·2023-02-10

    Mercedes-Benz Recalls 2022 EQS 580 for Windshield Camera Attachment Defect

    Mercedes-Benz is recalling 2022 EQS 580 vehicles because the windshield-mounted camera and rearview mirror may detach, potentially impairing air bag deployment and driver assistance systems.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580
    Category
    Vehicle
    Distribution
    Distributed nationwide