State

Texas product recalls

73,503 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.

Which agencies issued them

These figures cover only the 12,437 recalls whose distribution notice names Texas specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25201–25225 of 85940

SevereFDA (Drugs)·D-0421-2022·2022-02-02
Sterile Ophthalmic Solution Lacks Assurance of Sterility
Edge Pharma is recalling a sterile ophthalmic solution due to lack of assurance of sterility. The recall affects 2,562 syringes distributed nationwide.
Product
Phenylephrine HCl/Tropicamide/Cyclopentolate HCl/Ketorolac Sterile Ophthalmic Solution, 2.5%/0.25%/0.25%/0.125%, 0.5 mL syringe, Single Use Syringe, For Topical Ophthalmic Use, NDC 05446-0993-01
Category
Drug
Distribution
Distributed nationwide
HighCPSC·22069·2022-02-02
SureClose READYFIT 180° Hinge-Closer Sets Recalled for Drowning Hazard
D&D Technologies is recalling about 1,500 SureClose READYFIT 180° hinge-closer sets because they can malfunction and fail to fully self-close gates, allowing unintended access to pools and posing injury and drowning hazards to young children.
Product
SureClose® READYFIT 180° Hinge-Closer Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0527-2022·2022-02-02
Velano PIVO Blood Collection Device 20G units recalled for incomplete package sealing
Velano Vascular is recalling 123,700 PIVO Blood Collection Device 20G units due to incomplete package sealing that could compromise sterile barriers and allow microbial contamination.
Product
PIVO Blood Collection Device 20G, REF: 202-0005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0397-2022·2022-02-02
Ceftazidime Sterile Ophthalmic Solution Lacks Sterility Assurance
Edge Pharma is recalling Ceftazidime sterile ophthalmic solution for intraocular injection due to lack of assurance of sterility. The recall affects 168 syringes distributed nationwide.
Product
Ceftazidime, Sterile Ophthalmic Solution for Injection, Preservative Free (11.25 mg/0.5 mL (22.5 mg/mL), 0.5mL single use syringe for Intraocular Injection, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446, NDC 05446-0733-01
Category
Drug
Distribution
Distributed nationwide
HighCPSC·22066·2022-02-02
Children's Robes Recalled for Flammability Standards Violation
BAOPTEIL-branded children's robes sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. About 3,800 units sold from December 2019 through August 2021 are affected.
Product
Children's Robes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0405-2022·2022-02-02
Methacholine Challenge Test Kit Recalled for Lack of Sterility Assurance
Edge Pharma, LLC is recalling Methacholine Challenge 5-Syringe Test Kits nationwide due to lack of assurance of sterility. The sterile inhalation solution may not meet sterility standards.
Product
Methacholine Challenge 5-Syringe Test Kit, Sterile Inhalation Solution, Preservative Free, 3 mL per syringe,(NDC 05446-1600-05), Kit includes; individual syringe: Methacholine Chloride,16 mg/mL (contains 48 mg) NDC 05446-1241-01; Methacholine Chloride 4 mg/mL (contains 12mg)…
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V052000·2022-02-02
2021 Porsche Taycan Recalled for Front and Rear Suspension Misalignment
Porsche is recalling one 2021 Taycan with misaligned front and rear suspension. The misalignment may cause uneven tire wear and increase crash risk.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2022·2022-02-02
Diagnostic Imaging Angiography System Software Defects Recalled by Siemens
Siemens is recalling 23 Artis icono angiography systems due to four software defects that could disable imaging, corrupt images, and cause unexpected shutdowns during patient procedures.
Product
Artis icono floor with software VE20C-diagnostic imaging angiography system Model: 11327700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0515-2022·2022-02-02
Siemens Diagnostic Angiography System Recalled for Multiple Software Defects
Siemens is recalling its Artis pheno diagnostic angiography system (12 units) due to four software defects that may prevent imaging, corrupt images, or cause unintended shutdowns during clinical use.
Product
Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V055000·2022-02-02
2020-2022 Tiffin Allegro Red motorhome patio awning may detach during motion
Tiffin is recalling 2020-2022 Allegro Red motorhomes because the patio awning may have been improperly installed and could detach while driving, increasing crash and injury risk.
Product
TIFFIN — TIFFIN ALLEGRO RED
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0516-2022·2022-02-02
Artis icono diagnostic imaging system software defects recalled nationwide
Siemens is recalling 72 units of Artis icono biplane diagnostic imaging systems nationwide due to four software issues that could disable x-ray capability, corrupt diagnostic images, or cause unexpected shutdowns during procedures.
Product
Artis icono biplane with software VE20C-diagnostic imaging angiography system Model: 11327600
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V048000·2022-02-02
2021-2022 Keystone RV models recalled for tire belt separation defect
Keystone is recalling 2021-2022 Raptor and 2021 Montana RVs with certain Sailun tires that may experience belt separation. Belt separation could cause loss of vehicle control and increase crash risk.
Product
KEYSTONE — KEYSTONE RAPTOR, MONTANA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0522-2022·2022-02-02
GAT SPORT JETFUEL DIURETIC dietary supplement recalled for undeclared milk
World Health Products LLC is recalling GAT SPORT JETFUEL DIURETIC capsules because they may contain undeclared milk, a common allergen. The product was distributed across most U.S. states and internationally.
Product
GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal Actives; 90 Oil-Infused Capsules; Dietary Supplement; Other Ingredients: Gelatin (Capsule), Dicalcium Phosphate, Microcrystalline Cellulose, Magnesium Stearate…
Category
Food
Distribution
39 states
HighFDA (Drugs)·D-0417-2022·2022-02-02
Phenylephrine HCl Injection Recalled Due to Lack of Sterility Assurance
Edge Pharma is recalling approximately 5,335 syringes of Phenylephrine HCl Sterile Solution for Injection nationwide due to lack of assurance of sterility. The product may not meet sterility requirements for safe use.
Product
Phenylephrine HCl, Sterile Solution for Injection, (PF), 800 mcg/10mL (80 mcg/mL), Single Use Syringe for IV Injection, Edge Pharma, LLC 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1652-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0420-2022·2022-02-02
Edge Pharma Phenylephrine/Tropicamide Ophthalmic Solution Sterility Recall
Edge Pharma is recalling a sterile ophthalmic solution (Phenylephrine HCl/Tropicamide 2.5%/1%) because the manufacturer cannot assure sterility of the product. The recall affects 363 droptainers distributed nationwide.
Product
Phenylephrine HCl/Tropicamide, Sterile Ophthalmic Solution, 2.5%/1%, 15 mL per dropper, Multiple Dose Droptainer for Topical Ophthalmic Use, Edge Pharma, LLC, 856 Colchester, VT 05446, NDC 05446-0815-01
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V050000·2022-02-02
Tesla Model Y, S, X, and 3 windshield defrosting software defect
Tesla is recalling 2020-2022 Model Y, S, X, and 3 vehicles due to a heat pump software error that reduces windshield defrosting performance. This may decrease driver visibility and increase crash risk.
Product
TESLA — TESLA MODEL S, MODEL Y, MODEL 3, MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0615-2022·2022-02-02
Brownie Points Schmurtle Brownies Recalled for Undeclared Peanut Allergen
Brownie Points LLC is recalling Brownie Points Schmurtle brownies because the label does not disclose peanuts as an allergen. The product was distributed across the United States in gift baskets.
Product
Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually
Category
Food
Distribution
46 states
HighCPSC·22067·2022-02-02
Games Workshop Recalls KOYO Bounca The Squig Plush Toys for Choking Hazard
Games Workshop is recalling about 2,600 KOYO Bounca The Squig Limited Edition Plush toys because the pom-poms can detach, posing a choking hazard to young children. No injuries have been reported.
Product
KOYO Bounca The Squig Limited Edition Plush toys
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0406-2022·2022-02-02
Methotrexate Injection Recalled Due to Lack of Sterility Assurance
Edge Pharma, LLC is recalling Methotrexate, USP, Sterile Solution for Injection (125 mg/5mL) due to lack of assurance of sterility. The recall affects 457 syringes distributed nationwide.
Product
Methotrexate, USP, Sterile Solution for Injection (PF), 125 mg/5mL (2mg/mL), 5 mL per syringe, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-1505-05
Category
Drug
Distribution
Distributed nationwide
HighCPSC·22068·2022-02-02
Maxtrade Youth ATVs Recalled for Speed and Brake Safety Defects
About 141,000 Maxtrade Coolster Mountopz youth all-terrain vehicles fail to meet federal safety standards. The ATVs exceed maximum speed limits for their intended age groups and some have parking brakes that do not prevent vehicle movement, posing a risk of serious injury or death.
Product
Maxtrade's Youth Coolster Mountopz All-Terrain Vehicles (ATVs)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0524-2022·2022-02-02
GE Vscan Extend ultrasound device recalled for power-on failure due to battery depletion
GE Healthcare is recalling the Vscan Extend ultrasound device because it will not power on when the battery is depleted. This occurs when the device is not turned off before battery removal or is connected to a computer without AC power.
Product
GE Vscan Extend, being sold as "Vscan Extend Sector Wi-Fi"
Category
Medical Device
Distribution
50 states
HighFDA (Drugs)·D-0423-2022·2022-02-02
Betadine Sterile Ophthalmic Solution Recalled for Sterility Assurance
Edge Pharma is recalling Betadine sterile ophthalmic solution syringes due to lack of assurance of sterility. The affected product is a preservative-free, single-use ophthalmic solution distributed nationwide.
Product
Betadine (povidone-iodine), Sterile Ophthalmic Solution, Preservative Free, 5% 0.5mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446, NDC 05446-1680-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0403-2022·2022-02-02
Gemcitabine Intravesical Solution Recalled for Lack of Sterility Assurance
Edge Pharma is recalling approximately 627 syringes of Gemcitabine Sterile Intravesical Solution nationwide because the manufacturer cannot guarantee the product is sterile. The recalled batches were distributed between December 2021 and February 2022.
Product
Gemcitabine, Sterile Intravesical Solution, Preservative Free, 1g/50mL (20 mg/mL), 50 mL per syringe, Single Dose Syringe for Intravesical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1566-50
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0443-2022·2022-02-02
Phenol Topical Solution recalled for CGMP manufacturing deviations
Edge Pharma, LLC is recalling 1,861 vials of Phenol, Topical Solution (PF) 89%, 3 mL per vial, distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Phenol, Topical Solution (PF) Multiple Dose Vial, 89%, 3 mL per vial, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT, NDC 05446-1211-03
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0438-2022·2022-02-02
Lidocaine HCl / Oxymetazoline HCl Nasal Solution Recalled for CGMP Deviations
Edge Pharma, LLC is recalling Lidocaine HCl / Oxymetazoline HCl Nasal Solution (4% / 0.05%, 240mL) nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Lidocaine HCl / Oxymetazoline HCl Nasal Solution, 4% / 0.05%, 240mL per bottle, Multiple Dose Container for Intranasal Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1256-01, packaged in bottles. no label
Category
Drug
Distribution
Distributed nationwide