The Recall Desk

State

Texas product recalls

73,584 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
1,716
Severe
2,930
Most recent
2026-10-21

Of the 12,438 recalls naming Texas we have scored against our rubric, 1,716 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,930 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29001–29025 of 86022

  • ModerateFDA (Food)·F-0429-2021·2021-04-21

    J-Basket Seaweed Snack Recalled for Undeclared Food Dyes

    JFC International is recalling J-Basket Premium Korean Seaweed Snack because Wasabi flavor packages were incorrectly labeled as Original, failing to declare FD&C Yellow 5 and FD&C Blue No 1.

    Product
    J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer wrap for 3 inner packages Inner packages labeled J-Basket Premium Seaweed Snack - Original. Net Wt 0.52 oz. (15g) 3-0.17 oz. (5g) packs Distributed by JFC International Inc., Los Angeles, CA 90040 Wasabi outer…
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Drugs)·D-0360-2021·2021-04-21

    Spartan Chemical Recalls foamyiQ Hand Sanitizer Due to Manufacturing Deviations

    Spartan Chemical Company is voluntarily recalling 26,328 cartridges of foamyiQ Lemon Blossom Hand Sanitizer due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    foamyiQ Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%), Net Contents: 42.27 oz/1250 ml per foam pump cartridge, For Institutional and Industrial Use Only, Spartan Chemical Company, Inc., 1110 Spartan Drive, Maumee, OH 43537 USA. UPC 7 53727 26454 4 NDC: 64009-202-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0363-2021·2021-04-21

    Spartan Chemical Recalls Lite'n Foamy Handwash Due to Manufacturing Deviations

    Spartan Chemical Co Inc is voluntarily recalling 1,200 cases of Lite'n Foamy Eucalyptus Mint Sanitizing Handwash due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    LITE NFOAMY EUCALYPTUS MINT SANITIZING HANDWASH — LITE NFOAMY EUCALYPTUS MINT SANITIZING HANDWASH (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1424-2021·2021-04-21

    Remel Haemophilus Test Medium Recalled Due to Growth Issues

    Remel Inc is recalling 408 units of Haemophilus Test Medium because lighter-than-normal growth may make antimicrobial test zones difficult to measure.

    Product
    Remel Haemophilus Test Medium (150 mm) 10/PK, REF 04033 Remel Haemophilus Test Medium (HTM) is a solid medium recommended for use in qualitative procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0364-2021·2021-04-21

    Spartan Chemical Recalls Lite'n Foamy Handwash Due to CGMP Deviations

    Spartan Chemical Co Inc is voluntarily recalling 960 containers of Lite'n Foamy Healthcare Personnel Handwash due to CGMP deviations. The product was distributed nationwide in the US, Puerto Rico, and Mexico.

    Product
    LITE NFOAMY HEALTHCARE PERSONNEL HANDWASH — LITE NFOAMY HEALTHCARE PERSONNEL HANDWASH (CHLOROXYLENOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0362-2021·2021-04-21

    Spartan Chemical Recalls Lite'n Foamy E2 Sanitizing Handwash Due to CGMP Deviations

    Spartan Chemical Co Inc is voluntarily recalling 2,152 containers of Lite'n Foamy E2 Sanitizing Handwash due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    LITE NFOAMY E2 SANITIZING HANDWASH — LITE NFOAMY E2 SANITIZING HANDWASH (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1416-2021·2021-04-21

    Becton Dickinson Recalls BioGX SARS-CoV-2 Reagents for Sealed Tube Defect

    Becton Dickinson is recalling BioGX SARS-CoV-2 Reagents for BD MAX System because rehydration buffer tubes were not adequately sealed, potentially causing unresolved test results.

    Product
    BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0617-2021·2021-04-21

    Novo Nordisk Recalls OZEMPIC Injection Pens Due to Temperature Abuse

    Novo Nordisk is recalling OZEMPIC sample pens stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.

    Product
    OZEMPIC (semaglutide) injection, 2 mg/1.5 mL (1.34 mg/mL) Prefilled pen, 1 pen, Sample. Not for Resale, Rx only, Novo Nordisk Inc, Plainsboro, NJ 08536, Manufactured by: Novo Nordisk A/S, Bagsvaerd, Denmark, NDC 0169-4132-90 (Pen), NDC 0169-4132-97 (Kit)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0333-2021·2021-04-21

    Jubilant Cadista Recalls Itraconazole Capsules Due to Dissolution Failures

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Itraconazole Capsules, 100 mg, because they failed to meet dissolution specifications.

    Product
    Itraconazole Capsules, 100 mg, 30-count bottles, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-282-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2021·2021-04-21

    Biomerieux Recalls VIDAS CMV IgM Tests Due to Calibration Issues

    Biomerieux is recalling VIDAS CMV IgM test kits due to reported calibration issues. The recall affects 18,705 kits distributed nationwide and internationally.

    Product
    VIDAS¿ CMV IgM 30 Tests
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1425-2021·2021-04-21

    Remel Haemophilus Test Medium Recalled for Reduced Organism Growth

    Remel Inc is recalling 19 units of Haemophilus Test Medium because lighter-than-normal growth may make antimicrobial test zones difficult to measure.

    Product
    Remel Haemophilus Test Medium(100mm) 10/PK, REF: R01503 Remel Haemophilus Test Medium (HTM) is a solid medium recommended for use in qualitative procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1430-2021·2021-04-21

    Boston Scientific Recalls MAMBA Microcatheters for Labeling Errors

    Boston Scientific is recalling 63 MAMBA Microcatheters due to incorrect labeling and packaging. The devices were distributed nationwide and internationally.

    Product
    MAMBA Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then labeled and placed in carton with IFU. A closure strip, top and side labels are applied to the carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1429-2021·2021-04-21

    Boston Scientific Recalls MAMBA Flex 135 Microcatheters for Labeling Errors

    Boston Scientific is removing specific batches of MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.

    Product
    MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then labeled and placed in carton with IFU. A closure strip, top and side labels are applied to the carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1406-2021·2021-04-21

    Centinel Spine Recalls Prodisc C Devices Missing Orientation Marking

    Centinel Spine is recalling 49 Prodisc C cervical disc prostheses because the 'UP' orientation marking is missing from the superior plate.

    Product
    Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following single-level discectomy for intractable symptomatic cervical disc disease (SCDD), Part number: 09.820.055S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1380-2021·2021-04-21

    Arthrex Recalls Tibial Opening Wedge Osteotomy Plates Due to Processing Error

    Arthrex, Inc. is recalling 32 units of Tibial Opening Wedge Osteotomy Plates because five parts were incorrectly processed as a different model.

    Product
    Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and fractures of the proximal tibia and distal femur.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1417-2021·2021-04-21

    Vectornate Recalls MedSchenker Smart Transport Medium Due to Discoloration

    Vectornate USA Inc is recalling 130,000 MedSchenker Smart Transport Medium systems due to discoloration and turbidity caused by a longer monsoon season at the manufacturing facility.

    Product
    MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA, NON-SELECTIVE AND NON-DIFFERENTIAL - MULTIPURPOSE CULTURE MEDIUM - Product Usage: intended for the collection and transport of clinical specimens containing viruses, from the collection site to the testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0331-2021·2021-04-21

    Teligent Pharma Recalls Lidocaine Ointment for Failed Stability Specifications

    Teligent Pharma is recalling Lidocaine Ointment USP, 5%, due to failed viscosity specifications. The recall covers 62,040 tubes distributed nationwide.

    Product
    Lidocaine Ointment USP, 5%, NET WT 35.44 g (1 1/4 Oz) tube, Rx Only, Teligent Pharma Inc., Buena, New Jersey, 08310, NDC 52565-008-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E032000·2021-04-20

    Cummins Diesel Engine Fuel Rail Recall for Fire Risk

    Cummins is recalling specific L9 and ISX12 diesel engines because a sealing washer defect may cause fuel leaks, increasing the risk of fire.

    Product
    FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V269000·2021-04-20

    Manac Recalls 2018-2019 Trailers Due to Potential Steering Arm Detachment

    Manac is recalling 2018-2019 Steel Platforms, Transfer Trailers, and Square Dump Trailers because steer arm bolts may break, allowing the arm to detach and drag.

    Product
    MANAC — MANAC SQUARE DUMP TRAILER, STEEL PLATFORM, TRANSFER TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E030000·2021-04-16

    TSE Brakes Recalls Omni Tandem Brake Chambers Due to Spring Defect

    TSE Brakes is recalling certain Omni Tandem Brake Chambers because incorrect springs may cause the pressure plate to shift, potentially leading to a loss of air pressure and increased crash risk.

    Product
    PARKING BRAKE:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E029000·2021-04-16

    Daimler Trucks Recalls Detroit Axles Due to Steering Bolt Defect

    Daimler Trucks North America is recalling Detroit Model 2 and 3 axles because steering arm and tie rod bolts may fracture, potentially causing a loss of steering.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E028000·2021-04-16

    Meritor Recalls 14Xe ePowertrains Due to Electrical System Defect

    Meritor is recalling specific 14Xe ePowertrains because insufficiently crimped stator wires may cause overheating and loss of motive power, increasing crash risk.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide