Texas recalls
3,739 federal recalls affecting Texas in the last 12 months - 377 Texas-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-17FDA-DeviceD.O.R.CClass IINationwideD.O.R.C. TDC VELOCE cutter recalled for loose knife risk
D.O.R.C. has recalled certain TDC VELOCE 23G Two Dimensional Cutters used in ophthalmic surgery because the outer knife can become loose during use. An increased number of complaints about this issue prompted the recall. No injuries have been reported.
- 2026-06-17FDA-DeviceFresenius Medical CareClass IINationwideFresenius Bicarby Dialysate recalled for leak and slip hazard
Fresenius Medical Care is notifying users of potential leaks in Bicarby Dialysate products during setup and use. Fluid leaks from the luer-lock connection can create a slip and fall hazard on the floor where treatment is taking place.
- 2026-06-17FDA-DeviceBerlin HeartClass IINationwideBerlin Heart EXCOR Pediatric VAD blood pump recalled for expiration date mismatch
Some Berlin Heart EXCOR Pediatric Ventricular Assist Device blood pumps have mismatched expiration dates between the inner and outer package labels. The inner package shows an incorrect expiration date, which could cause confusion and delay surgical procedures if the device is not used on time.
- 2026-06-17FDA-DeviceMozarc MedicalClass IINationwideMahurkar Elite PASS Trays recalled for missing dressing
Certain lots of Mozarc Medical's Mahurkar Elite PASS Trays are missing the Tegaderm CHG antimicrobial dressing that is supposed to be included in the kit. These trays are used in hospitals and clinical settings for acute hemodialysis, aphaeresis, and infusion procedures. The missing dressing may affect the product's intended sterile barrier protection.
- 2026-06-17FDA-DeviceGEClass IINationwideGE Allia Moveo X-ray system recalled for electrical shock risk
GE HealthCare identified a potential electrical cable issue on certain Allia Moveo angiographic X-ray systems equipped with Gaia generators. Service personnel who work inside the equipment cabinet while power is on could be exposed to electrical shock during installation, maintenance, or troubleshooting.
- 2026-06-17FDA-DeviceGEClass IINationwideGE Allia IGS Pulse X-ray system recalled for electrical shock risk
GE HealthCare identified a potential electrical cable issue on certain Allia IGS Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel performing installation, maintenance, or troubleshooting work inside the C-FRT cabinet while power is on could be exposed to electrical shock.
- 2026-06-17FDA-DeviceGEClass IINationwideGE Allia IGS 7 Pulse X-ray system recalled for electrical shock risk
GE HealthCare identified a faulty electrical cable on certain Allia IGS 7 Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel working inside the C-FRT cabinet while the system is powered on could receive an electrical shock during installation, maintenance, or troubleshooting.
- 2026-06-17FDA-DeviceGEClass IINationwideGE Allia IGS 5 Pulse X-ray system recalled for electrical shock risk
GE HealthCare identified a potential electrical cable issue on certain Allia IGS 5 Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel performing installation, maintenance, or troubleshooting inside the C-FRT cabinet while power is on face a risk of electrical shock.
- 2026-06-17FDA-DeviceGEClass IINationwideGE HealthCare Allia IGS 3 Pulse X-ray system recalled for electrical shock risk
GE HealthCare identified a potential electrical cable issue on certain Allia IGS 3 Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel performing installation, maintenance, or troubleshooting work inside the C-FRT cabinet while the system is powered on could be at risk of electrical shock.
- 2026-06-17FDA-DeviceICU MedicalClass IINationwideICU Medical Plum Duo IV Pump recalled for alert display failure
The Plum Duo Precision IV Pump may fail to display a soft limit alert under certain conditions, meaning clinicians won't be notified before the pump starts delivering medication that exceeds the set safety limit. This could result in patients receiving too much or too little medication.
- 2026-06-17FDA-DeviceICU MedicalClass IINationwideICU Medical Plum Duo pump recalled for missing alerts
The Plum Duo Infusion Pump may fail to display alerts when medication delivery limits are exceeded. Without these warnings, clinicians may not know before the pump starts delivering the wrong amount of medication to a patient.
- 2026-06-17FDA-DeviceICU MedicalClass IINationwideICU Medical Plum Solo IV Pump recalled for missed alerts
The Plum Solo Precision IV Pump may fail to display a soft limit alert under certain conditions, preventing clinicians from being notified of dosage limit violations before the pump starts delivery. This could result in incorrect medication doses being administered.
- 2026-06-17FDA-DeviceFresh Roast SystemsClass IINationwideFresh Roast Systems ColorTrack recalled for laser exposure risk
A manufacturing defect in the Fresh Roast Systems ColorTrack model BENCH R-100 could, under rare misuse conditions, expose users to infrared laser light levels higher than the product's safety rating. No injuries have been reported. The defect affects a small number of units.
- 2026-06-17FDA-FoodE & S Grocery & BakeryClass IE & S Grocery & Bakery taro cakes recalled for undeclared egg
E & S Grocery & Bakery taro cakes contain egg but the packaging does not declare it as an allergen. The recall affects all lot codes of the product (UPC #652565100055). About 300 units were distributed across eight states.
- 2026-06-17FDA-FoodU.S. TradingClass IIDRAGONFLY Thai Ginger Powder recalled for lead contamination
U.S. Trading Company is recalling DRAGONFLY Thai Ginger Powder (4.37 oz) because it may contain lead. The powder was distributed across multiple U.S. states. No injuries have been reported.
- 2026-06-17FDA-FoodTotal NutritionClass INationwideTotal Nutrition moringa capsules recalled for Salmonella risk
Total Nutrition Inc is recalling TNVitamins and Doctor's Pride brand moringa capsule supplements because they may be contaminated with Salmonella. The recall affects 13,000 bottles sold nationwide across multiple lot numbers.
- 2026-06-17FDA-FoodBEF FoodsClass IINationwidePark St. Deli mac and cheese recalled for undeclared soy
Park St. Deli Macaroni & Cheese (20 oz packages) contains soy lecithin that is not listed on the label. People with a soy allergy or sensitivity could have a serious reaction if they eat this product without knowing soy is present.
- 2026-06-17FDA-FoodHH FreshClass IHH Fresh enoki mushrooms recalled for Listeria risk
HH Fresh Trading Corp. enoki mushrooms (150g packages) tested positive for Listeria monocytogenes, a harmful bacterium. The product was distributed to Texas and Florida. No illnesses have been reported so far.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Flan Cake recalled for undeclared dyes
Galaxy RG Corp's Flan Cake Custard Cake (30 oz) contains food dyes—Yellow #5, Yellow #6, and/or Red #40—that are not listed on the label. The affected products were sold in Florida and Texas with expiration dates between April 3 and May 3, 2026.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Guava Cheesecake recalled for undeclared dyes
Galaxy RG Corp's Cheesecake de Guava (26 oz) contains food coloring dyes (Yellow #5, Yellow #6, and/or Red #40) that are not listed on the label. People with allergies or sensitivities to these dyes could have a reaction if they consume the product without knowing the dyes are present.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp strawberry cheesecake recalled for undeclared dyes
Galaxy RG Corp's Cheesecake de Fresa strawberry cheesecake (26 oz) contains undeclared food dyes: Yellow #5, Yellow #6, and/or Red #40. These dyes are not listed on the package label. Certain lots distributed in Florida and Texas between April and May 2026 are affected.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Mango Cheesecake recalled for undeclared dyes
Galaxy RG Corp's Mango Cheesecake (26 oz) contains food dyes Yellow #5, Yellow #6, and/or Red #40 that are not listed on the label. The affected product was distributed in Florida and Texas with expiration dates between April 3 and May 3, 2026.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp caramel cheesecake recalled for undeclared dyes
Galaxy RG Corp's Cheesecake de Dulce de Leche Caramel Cheesecake (26 oz) contains food dyes—Yellow #5, Yellow #6, and/or Red #40—that are not listed on the label. People with dye allergies or sensitivities may have a reaction if they consume this product without knowing the dyes are present.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Marquesita cakes recalled for undeclared dyes
Galaxy RG Corp's Marquesita de Chocolate y Vainilla Delighted Flavored Cakes contain undeclared food coloring (Yellow #5, Yellow #6, and/or Red #40) that is not listed on the label. People with allergies or sensitivities to these dyes could have a reaction if they consume the product without knowing the dyes are present.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Marquesita de Dulceleche cakes recalled for undeclared dyes
Galaxy RG Corp's Marquesita de Dulceleche Delighted Flavored Cakes (16 oz) contain undeclared food coloring: Yellow #5, Yellow #6, and/or Red #40. These dyes are not listed on the package label. The affected cakes were sold in Florida and Texas with expiration dates from April 3, 2026 to May 3, 2026.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Marquesita de Fresa cakes recalled for undeclared dyes
Galaxy RG Corp's Marquesita de Fresa Delighted Flavored Cakes (16 oz) contain undeclared food dyes—Yellow #5, Yellow #6, and/or Red #40—that are not listed on the package label. This poses a risk to people with allergies or sensitivities to these colorants. The affected products were distributed in Florida and Texas with expiration dates between April 3 and May 3, 2026.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Marquesita de Mango cakes recalled for undeclared colors
Galaxy RG Corp is recalling Marquesita de Mango Delighted Flavored Cakes because they contain undeclared food colors (Yellow #5, Yellow #6, and/or Red #40) that are not listed on the label. People with allergies or sensitivities to these dyes may be at risk if they consume the product unknowingly.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp guava cakes recalled for undeclared dyes
Galaxy RG Corp's Marquesita de Guava Delighted Flavored Cakes contain undeclared food coloring (Yellow #5, Yellow #6, and/or Red #40) that is not listed on the label. The affected cakes were sold in 16-oz containers with expiration dates between April 3, 2026 and May 3, 2026 in Florida and Texas. This poses a risk to people with allergies or sensitivities to these dyes.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Tiramisu Coffee Cake recalled for undeclared dyes
Galaxy RG Corp's Tiramisu Coffee Cake (30 oz) contains food dyes—Yellow #5, Yellow #6, and/or Red #40—that are not listed on the label. These dyes can trigger allergic reactions or other health effects in people with sensitivities or those who avoid them for medical reasons. The recall affects specific lot codes with expiration dates between April 3 and May 3, 2026, sold in Florida and Texas.
- 2026-06-17FDA-FoodGalaxyClass IIGalaxy RG Corp Cake de Mango recalled for undeclared food dyes
Galaxy RG Corp's Cake de Mango (47 oz) contains Yellow #5, Yellow #6, and/or Red #40 that are not listed on the label. These food colors can cause allergic reactions in people with sensitivities to synthetic dyes. The product was distributed in Florida and Texas with specific lot numbers and expiration dates between April 3 and May 3, 2026.
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