The Recall Desk

State

Texas product recalls

73,495 recalls have nationwide distribution and so reach Texas. 12,437 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,437
Critical
1,720
Severe
2,926
Most recent
2026-10-14

Of the 12,437 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.

These figures cover only the 12,437 recalls whose distribution notice names Texas specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24526–24550 of 85932

  • HighFDA (Devices)·Z-0727-2022·2022-03-16

    B. Braun dispensing pins recalled for air filter leakage risk

    B. Braun Medical is recalling dispensing pins with an elevated leakage risk in the air inlet filter. The leakage may reduce medication doses, delay treatment, or contaminate the fluid path, potentially causing bloodstream infection.

    Product
    Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration or injection of medication or enteral feeding solution from inverted multi-dose vials.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0743-2022·2022-03-16

    Medtronic endotracheal tubes recalled due to manufacturing nonconformity

    Medtronic Xomed is recalling over 301,000 NIM TRIVANTAGE EMG Endotracheal Tubes due to a manufacturing nonconformity. These devices were distributed worldwide.

    Product
    NIM TRIVANTAGE EMG Endotracheal Tube
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0725-2022·2022-03-16

    Philips X-ray System Cooling Leak Poses Fire Risk

    Philips Allura CV20 X-ray systems with certain Laird chillers may leak cooling liquid onto electrical components, potentially causing fire or smoke. Affected systems should not be operated until the issue is addressed.

    Product
    Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0732-2022·2022-03-16

    Radiation therapy planning software displays wrong images during animation playback

    RayStation/RayPlan versions 6.0.0.24 through 9.2.0.483 incorrectly display selected images as both primary and secondary when animation playback is running, affecting treatment planning visualization.

    Product
    RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 .…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0724-2022·2022-03-16

    Philips Allura Xper X-ray systems cooling system leak poses fire risk

    Philips Allura Xper interventional X-ray systems may experience cooling liquid leaks that could drip on electrical components, creating risk of fire, smoke, or burning odors. No injuries have been reported.

    Product
    Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray: Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0738-2022·2022-03-16

    FDA Recalls Diagnostic Test Strips for False Positive Results

    NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.

    Product
    NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pouches. Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0739-2022·2022-03-16

    Nextra CH Hammertoe Surgical Implant Kit Recalled for Locking Mechanism Defect

    Nextremity Solutions recalls the Nextra CH Hammertoe Mini Instrument Kit for a defect that may deform the implant's locking mechanism during insertion, potentially requiring revision surgery.

    Product
    Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes SKU: CH-MINI-KT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0729-2022·2022-03-16

    Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications

    A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.

    Product
    HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0856-2022·2022-03-16

    Dry Salted Plum with Chili Products Recalled for Potential Lead Contamination

    El Super Leon and El Leoncito brand Dry Salted Plum with Chili products are recalled due to potential lead contamination. Consumers should not consume these products.

    Product
    El Super Leon brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag, Net Wt 1.05oz, UPC 8-52605-00408. With 12 packs of 12 units per case, for a total of 144 units per case. El Leoncito brand, Dry Salted Plum with Chili, Shelf Stable, packaged in plastic bag…
    Category
    Food
    Distribution
    6 states
  • HighCPSC·22103·2022-03-16

    B. toys Wooden Activity Walker recalled for choking hazard

    B. toys Walk 'n' Learn wooden toddler walkers are being recalled because wheels and attachment hardware can detach in small pieces, creating a choking hazard for young children. Battat has received six reports of detachment, including one incident where a child placed a detached metal nut in her mouth.

    Product
    B. toys Wooden Activity Walker - Walk 'n' Learn
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V162000·2022-03-16

    2021 Volkswagen ID.4 Battery Cell Soldering Defect Recall

    Volkswagen is recalling certain 2021 ID.4 vehicles due to improper soldering of the high-voltage battery connection. The defect may cause an unreliable connection that could lead to vehicle stalling and increase crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0823-2022·2022-03-16

    El Chavito Saladitos Enchilados Salted Plums Recalled for Potential Lead Contamination

    El Chavito Saladitos Enchilados Salted Plums (1.7 oz.) are being recalled nationwide due to potential lead contamination. Consumers should not consume this product.

    Product
    El Chavito¿ Saladitos Enchilados Salted Plums with Chili, net wt. 1.7 oz., Individual UPC 859470006070, Master Case UPC 859470006612.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0740-2022·2022-03-16

    Surgical hammertoe instruments recalled for potential locking mechanism deformation

    The Nextra Cannulated Hammertoe Standard Instrument Kit's driver may deform the implant locking mechanism during insertion, potentially requiring revision surgery.

    Product
    Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0828-2022·2022-03-16

    Dried Salted Plums Recalled for Elevated Lead Levels

    Pacific Golden Coast Trading Inc is recalling 820 cases of dried salted plums due to elevated lead levels. The product was distributed in California and Texas.

    Product
    Dried salted plum, packaged in 22 lbs. carton. Product of China.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0855-2022·2022-03-16

    Dry Salted Plums Recalled Due to Potential Lead Contamination

    El Super Leon Ponchin Snacks is recalling EL Leoncito and El Super Leon brand dry salted plums due to potential lead contamination. Consumers should not consume these products.

    Product
    EL Leoncito brand Dry Salted Plum, Shelf Stable, packaged in plastic bag, Net Wt 1.4oz, UPC 8-52605-00024. 12 packs with 12 units per case - 144 total units El Super Leon brand Dry Salted Plum, Shelf Stable, packaged in plastic bag, Net Wt 1.4oz, UPC 8-52605-00407. The label…
    Category
    Food
    Distribution
    6 states
  • HighCPSC·22099·2022-03-16

    Reckitt Recalls 3.74 Million Bottles of Airborne Gummies for Pressure Hazard

    RB Health (Reckitt) is recalling approximately 3.74 million bottles of Airborne Gummies (63 and 75 count) because pressure buildup can cause the cap and seal to pop off with force upon first opening, posing an injury hazard.

    Product
    Airborne Gummies (63 and 75 count bottles)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2022·2022-03-16

    Laboratory diagnostic tips recalled for potential dispensing errors

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry VersaTips due to shape deformity that may reduce sample volume by 16%. Undetected errors could result in inaccurate test results for bloodborne infectious disease assays.

    Product
    VITROS Chemistry Products VersaTips, Catalog No. 6801715 A VersaTip sales unit is composed of 1000 tips per box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0822-2022·2022-03-16

    El Chavito Saladitos Dried Salted Plums Recalled for Potential Lead Contamination

    El Chavito Saladitos Dried Salted Plums are being recalled due to potential lead contamination. The recall affects 37,552 packages distributed nationwide.

    Product
    El Chavito¿ Saladitos Dried Salted Plums, net wt. 1.7 oz bag, Individual UPC 859470006049, Master Case UPC 859470006629. El Chavito¿ Saladitos Dried Salted Plums, net wt. 1.7 oz bag, Individual UPC 850013297221, Master Case UPC 850013297726.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·22104·2022-03-16

    Prestone Shop Pro RV & Marine Antifreeze Recall for Methanol Poisoning Risk

    Prestone has recalled Shop Pro RV & Marine Antifreeze sold at AutoZone after discovering some bottles were improperly filled with methanol-containing product and lack required hazard warnings. Methanol can cause poisoning through inhalation or ingestion and may be fatal or cause blindness.

    Product
    Shop Pro RV & Marine Antifreeze
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0728-2022·2022-03-16

    Stryker Camera Control Unit Recalled Due to Inverted Image Display Defect

    Stryker is recalling the 1688 Camera Control Unit due to a software defect that causes the surgical monitor image to flip upside-down. This could lead to surgeon error or the need for additional surgical intervention.

    Product
    1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear endoscopy, sinuscopy, and plastic surgery wherever a laparoscope/endoscope/arthroscope/sinuscope is used.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0746-2022·2022-03-16

    PCA 4000 Dental Curing Units May Not Fully Cure Resins

    Envisiontec is recalling 172 PCA 4000 curing units that may not properly cure dental resins to specification (SKU ACC-06-1000).

    Product
    PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold to industrial customers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22100·2022-03-16

    Specialized Bicycle Crank Arm Disengagement Recall Poses Fall Hazard

    Specialized is recalling about 19,000 Sirrus bicycles with defective alloy cranks that can disengage and cause falls. The manufacturer has received 30 reports of the defect, but no injuries have been reported.

    Product
    Sirrus, Sirrus X and Sirrus Sport Bicycles with alloy cranks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22102·2022-03-16

    RH Illuminated Mirrors Recalled Due to Fire and Shock Hazards

    RH is recalling about 3,300 illuminated mirrors sold from September 2015 through February 2022 due to loose components in bulb sockets that can cause overcurrent, overheating, fire, and electrical shock. Consumers should stop using them immediately and contact RH for a refund or replacement.

    Product
    Illuminated Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V160000·2022-03-16

    Harley-Davidson Motorcycles Recalled for Detaching Brake Fluid Warning Labels

    Harley-Davidson is recalling certain 2021-2022 XL Sportster motorcycles because brake fluid warning labels may detach from reservoir caps. Missing labels could lead to improper brake maintenance and increased crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XL883N, XL1200X, XL1200NS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0649-2022·2022-03-16

    Paliperidone Extended-Release Tablets Recalled for Failed Dissolution

    The Harvard Drug Group is recalling 174 cartons of Paliperidone Extended-Release Tablets, 9 mg, nationwide due to failed dissolution specifications. The affected lots are N00522 (Exp. 09/2022) and N00618 (Exp. 11/2022).

    Product
    PALIPERIDONE — PALIPERIDONE (PALIPERIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide