The Recall Desk

State

Texas product recalls

72,940 recalls have nationwide distribution and so reach Texas. 12,389 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,389
Critical
1,705
Severe
2,407
Most recent
2026-09-09

Of the 12,389 recalls naming Texas we have scored against our rubric, 1,705 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,407 (19%) are Severe.

These figures cover only the 12,389 recalls whose distribution notice names Texas specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3751–3775 of 85329

  • HighCPSC·26226·2026-01-29

    Plush giraffe and llama toys recalled over legs that can detach

    About 21,230 Giraffe and Llama plush toys with clips sold at Hobby Lobby are being recalled because the legs can detach and release small beads.

    Product
    Giraffe Plush Toy with clip, Llama Plush Toy with clip
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26220·2026-01-29

    Electric bicycle rear wheel bolts recalled over breakage when torqued

    About 19,890 rear wheel bolts on 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles are being recalled because the bolts can break when torqued, causing wheel separation.

    Product
    Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V052000·2026-01-29

    Winnebago Recalls 2026 Access Travel Trailers for Missing Weight Label

    Winnebago is recalling 2026 Access travel trailers because the Gross Axle Weight Rating may be missing from the certification label, which could lead to overloading.

    Product
    WINNEBAGO — WINNEBAGO ACCESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26236·2026-01-29

    Cargo electric bicycles recalled over buckles that may not latch

    About 320 Urban Arrow FamilyNext Pro Cargo E-Bikes are being recalled because the Fidlock buckle can fail to fully latch when used with children in the cargo area.

    Product
    Urban Arrow FamilyNext Pro Cargo E-Bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26218·2026-01-29

    Hot water pressure washers recalled over fan wheels that can fail

    About 1,416 NorthStar hot water pressure washers are being recalled because the fan wheel can fail, causing abnormal burner operation that can produce smoke or bursts of flames.

    Product
    Sefudun Hair Growth Serum Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26222·2026-01-29

    Submersible LED lights recalled over accessible lithium coin batteries

    About 9,150 LuxJet Submersible LED Lights are being recalled because the lithium coin batteries can be accessed easily by children and the lights lack the warnings required by Reese's Law.

    Product
    LuxJet Submersible LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26227·2026-01-29

    Above-ground pools recalled over a compression strap that creates a foothold

    About 2,390 Sunneday and Blue Bay above-ground pools 48 inches and taller are being recalled because the compression strap around the pool legs may let a child climb in.

    Product
    Sunneday and Blue Bay brand 48-inch and taller above-ground pools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1147-2026·2026-01-28

    Full electric lightweight homecare beds recalled over pendants that may overheat

    Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP), non-inv
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V050000·2026-01-28

    Ducati motorcycle rear brake hose may fail from excessive heat

    Ducati is recalling certain 2025-2026 Streetfighter V4 and Panigale V4 motorcycles because excessive heat may damage the rear brake hose, resulting in a sudden loss of the rear brakes.

    Product
    DUCATI — DUCATI STREETFIGHTER V4, PANIGALE V4, STREETFIGHTER V4 S, PANIGALE V4 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1124-2026·2026-01-28

    Angiographic inflation devices recalled over handles that may detach

    Merit Medical Systems is recalling 173,645 units of the Allwell Inflation Device because the inflation device handle may detach from the syringe during a procedure.

    Product
    Allwell Inflation Device, for angiographic use REF: IS-30-A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0295-2026·2026-01-28

    Icosapent ethyl capsules recalled as subpotent after capsule contents leaked

    Zydus Pharmaceuticals is recalling 22,896 bottles of Icosapent Ethyl capsules, 1 gram, because oxidation caused by leakage of the capsule contents has left them subpotent.

    Product
    Icosapent Ethyl capsules, 1 gram, 120-count bottles, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1592-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V049000·2026-01-28

    Toyota Prius models recalled for unexpected rear door opening risk

    Toyota is recalling certain 2023–2026 Prius and Prius Prime models because water may enter the rear door switch, causing an unlocked door to open unexpectedly while driving. This increases injury risk.

    Product
    TOYOTA — TOYOTA PRIUS PLUG-IN HYBRID, PRIUS PRIME, PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2026·2026-01-28

    Custom inflation kits recalled over inflation handles that may detach

    Merit Medical Systems is recalling 18,897 units of its Custom Inflation Kit because the inflation device handle may detach from the syringe during a procedure.

    Product
    Merit Medical , Custom Inflation Kit REF: K05-00761F K05-01717B K05-02080D K05-02090C K05-02221 K05-02338 K05-02470 K05-02954 K05-03094A K05T-00380C K05T-01674B K05T-01863 K05T-01915 K05T-01920F K05T-01955 K05T-02138 K05T-02138A K05T-02272G K05T-02272H K05T-02533 K05T-03153 K05T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1112-2026·2026-01-28

    PET scanners recalled over a streaking artifact in clinical images

    GE HealthCare is recalling 364 Omni Legend PET systems because an intermittent issue can produce a streaking artifact in PET clinical scan images.

    Product
    GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend PET Gantry 16cm - MEA, Omni Legend PET Gantry 16cm Haifa LM, Omni Legend PET Gantry 16cm Mobile, Omni Legend PET Gantry 21cm - BJ for Global, Omni Legend PET
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1145-2026·2026-01-28

    Endoluminal vision probe bags recalled over compromised sterile pouch seals

    Intuitive Surgical is recalling 110,580 Ion Vision Probe Bags because the probe bags may have a compromised or incomplete sterile pouch seal.

    Product
    Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50, iM60, iM70, iM80 Product Description: The iM series Patient Monitor including iM50, iM60, iM70 and iM80 can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1135-2026·2026-01-28

    LDL cholesterol assays recalled over triglyceride interference causing biased results

    Beckman Coulter is recalling 34,451 units of the LDL Cholesterol OSR6x96 assay because triglyceride interference may cause a positive bias of up to 28.8% in low LDL cholesterol samples.

    Product
    The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol from non-LDL- lipoprotein particles. This cholesterol is consumed by cholesterol esterase, cholesterol oxidase, peroxidase and 4- aminoantipyrine to generate a c
    Category
    Medical Device
    Distribution
    52 states