State

Texas product recalls

73,088 recalls have nationwide distribution and so reach Texas. 12,427 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,427
Critical: 1,720
Severe: 2,421
Most recent: 2026-09-23

Of the 12,427 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 2,421 (19%) are Severe.

Which agencies issued them

These figures cover only the 12,427 recalls whose distribution notice names Texas specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9276–9300 of 85515

HighFDA (Drugs)·D-0140-2025·2024-12-25
Dental City Topical Anesthetic Gel Recalled Due to Manufacturing Defect
Dental City Topical Anesthetic Gel (Benzocaine 20%) is recalled because the product was released and distributed despite failing quality inspection. Scratches were found in the mixing vessel during routine inspection.
Product
Dental City, Topical Anesthetic Gel, Benzocaine 20%, Net Content: 1 oz. (30 ml), Gluten Free, Manufactured for: Dental City, Green Bay, WI 54311, dentalcity.com.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0692-2025·2024-12-25
K-Systems Incubator Device Recall: Temperature May Exceed Desired Setting
CooperSurgical is recalling 34 K-Systems incubator devices used in assisted reproduction procedures. The warming surfaces may exceed the desired set temperature, though the device will alarm if this occurs.
Product
Brand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number: Multiple/unknown Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g.,
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-0687-2025·2024-12-25
K-Systems G73 Dry Bath Incubator may exceed target temperature
CooperSurgical is recalling K-Systems G73 Dry Bath Incubators because warming surfaces may exceed the desired set temperature. The device alarms when this occurs.
Product
Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and embryos), at c
Category
Medical Device
Distribution
14 states
HighFDA (Drugs)·D-0138-2025·2024-12-25
Topical Anesthetic Gel Recalled for Manufacturing Equipment Defect
Keystone Industries is recalling Benzocaine 20% topical anesthetic gel due to scratches in the manufacturing mixing vessel. Despite Quality Assurance rejection, the product was inadvertently shipped to customers.
Product
M&S Dental Supply Co LLC., Topical Anesthetic Gel, Benzocaine 20%, Net Wt. 1 oz. (30ml), Manufactured for: M&S Dental Supply Co LL, 105-30 101 Avenue, Ozone Park, NY 11416.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0306-2025·2024-12-25
Griffith Foods Italian Style Herb Powder Recalled for Metal Contamination
Griffith Foods has recalled Item 79588401 (Italian Style Herb Powder) in 55 lb bags due to potential metal pieces. Affected lots 577773 and 577774 were distributed to IL, NY, NC, WI, TX, TN, and GA.
Product
Item 79588401, ITAL STY PD HERB REDUCED EX, 55 lb. bag
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-0705-2025·2024-12-25
OEC 9900 Mobile Fluoroscopic X-Ray System Recall for Sealing Defect
GE OEC Medical Systems is recalling 78 OEC 9900 Elite mobile fluoroscopy systems due to insufficient sealing of X-ray tubes. The defect can result in oil leaks and loss of fluoroscopic imaging capability.
Product
OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedures. Examples of clinical application ma
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0690-2025·2024-12-25
K-Systems T47 Warming Plate May Exceed Set Temperatures
CooperSurgical recalls K-Systems T47 Warming Plates because temperature may exceed the desired set value, potentially affecting biological materials. The device alarms appropriately when this occurs.
Product
Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23055 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes
Category
Medical Device
Distribution
14 states
HighFDA (Food)·F-0311-2025·2024-12-25
L'Oven Fresh KETO Tortilla Wraps recalled for possible metal contamination
Rise Baking Company is recalling L'Oven Fresh KETO Friendly Original 6 Tortilla Wraps sold at Aldi stores in five states due to potential metal contamination. Affected products carry specific Julian date codes from 24 302 to 24 311.
Product
L'Oven Fresh KETO Friendly Original 6 Tortilla Wraps. Net Wt. 7.8 oz(222g) UPC 4099100271348. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510. Product of Canada
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0704-2025·2024-12-25
Fluoroscopic X-Ray System Recalled for Insufficient X-Ray Tube Sealing
GE OEC Elite mobile fluoroscopic X-ray systems are recalled due to insufficient sealing of X-ray tubes, which can cause oil leaks and loss of imaging capability. Approximately 100 systems have been affected.
Product
OEC Elite REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0706-2025·2024-12-25
GE OEC 9800 X-Ray System Recalled for Insufficient Tube Sealing
GE OEC 9800 fluoroscopic X-ray systems are recalled due to insufficient sealing of X-ray tubes, which can result in oil leaks and loss of imaging capability. 25 systems distributed in the U.S. and internationally are affected.
Product
OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscop
Category
Medical Device
Distribution
45 states
HighFDA (Drugs)·D-0152-2025·2024-12-25
Ophthalmic solution recalled for lack of sterility assurance
Regener-Eyes ophthalmic solution is being recalled due to lack of sterility assurance. Approximately 170,812 bottles distributed nationwide are affected.
Product
LITE Regener-Eyes, Ophthalmic Solution (glycerin 0.4%), 3mL bottles, Distributed by: Regener-Eyes, Tampa, FL; Manufactured by: Regenerative Processing Plant, LLC, 34176 US HWY 19N, FL, NDC 82305-006-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0146-2025·2024-12-25
Quala Dental Topical Anesthetic Gel Recalled for Manufacturing Equipment Defect
Quala Dental Products topical anesthetic gel (20% benzocaine) is recalled due to manufacturing equipment defects. The bulk product was inadvertently released despite Quality Unit rejection after inspection found scratches on the mixing vessel.
Product
Quala Dental Products, Topical Anesthetic Gel, Contains 20% Benzocaine, Net Contents: 1 oz (30g), Gluten Free, Quala Dental Products, Made in USA for: NDC, Inc, 407 New Sanford Road, La Vergne, TN 37086, www.quala.com
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0151-2025·2024-12-25
VCF Contraceptive Pre-filled Applicators Recalled for Out-of-Specification Active Ingredient
Apothecus Pharmaceutical recalls 33,659 boxes of VCF nonoxynol-9 contraceptive gel nationwide due to out-of-specification active ingredient assay from manufacturing deviations. No illnesses reported.
Product
VCF CONTRACEPTIVE PRE-FILLED APPLICATORS — VCF CONTRACEPTIVE PRE-FILLED APPLICATORS (NONOXYNOL-9)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0688-2025·2024-12-25
K-Systems G85 Mini Incubator May Exceed Desired Temperature
CooperSurgical recalls 37 K-Systems G85 Mini Incubators because the device warming surfaces may exceed the desired set temperature. The unit alarms when this occurs, but affected serial numbers require verification.
Product
Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes
Category
Medical Device
Distribution
14 states
HighFDA (Food)·F-0284-2025·2024-12-25
Impossible Savory Ground Sausage Recalled Due to Potential Metal Contamination
Impossible Foods is recalling Impossible Savory Ground Sausage nationwide due to potential metal contamination. Consumers should not consume affected products and should return them to their retailer.
Product
Impossible Savory Ground Sausage Meat from plants 14oz chub, UPC 8 16697 02108 8; 8 retail chubs per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0307-2025·2024-12-25
Griffith Foods Breader Recalled for Potential Metal Contamination
Griffith Foods Ltd is recalling Item 25293502 Adhesion Breader EX due to potential pieces of metal in the product. The recall affects approximately 25,903 pounds distributed across multiple states.
Product
Item 25293502, ADHESION BREADER EX, 50 lb. bag
Category
Food
Distribution
7 states
HighFDA (Food)·F-0309-2025·2024-12-25
Bakestone Brothers Pita Bread recalled for metal contamination
Bakestone Brothers Pita Bread (6-count) is being recalled from five states due to metal fragments found in the product. Consumers should not consume the affected bread.
Product
Bakestone Brothers Pita Bread, 6 White Pita. Net Wt. 11.4 oz(325g) UPC 0 57391-00001 0. Manufactured by PBF pita Bread Factory Ltd, 8000 Winston Street, Burnaby British Columbia V5A 2H5. Product of Canada
Category
Food
Distribution
5 states
HighFDA (Drugs)·D-0144-2025·2024-12-25
Pearson Quality Topical Anesthetic Gel Recalled Due to Manufacturing Defect
Keystone Industries is recalling Pearson Quality Topical Anesthetic Gel (20% Benzocaine) due to manufacturing equipment defects that could allow product contamination. The affected lot was inadvertently shipped despite quality control rejection.
Product
Pearson Quality, Topical Anesthetic Gel, 20% Benzocaine, For Professional Use Only, Net Contents: 1 oz (30 g), Manufactured for Pearson Dental Supply Inc., Sylmar, CA 91342 USA.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0312-2025·2024-12-25
L'Oven Fresh KETO Tortilla Wraps Recalled for Metal Contamination
L'Oven Fresh KETO Friendly Multiseed 6 Tortilla Wraps are being recalled due to potential metal contamination. Products were distributed in CT, KS, MN, OH, and TX.
Product
L'Oven Fresh KETO Friendly Multiseed 6 Tortilla Wraps. Net Wt. 7.8 oz(222g) UPC 4099100271355. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510. Product of Canada
Category
Food
Distribution
5 states
HighFDA (Food)·F-0285-2025·2024-12-25
Impossible Spicy Ground Sausage Recalled for Potential Metal Contamination
Impossible Foods is recalling Impossible Spicy Ground Sausage due to potential metal pieces in the product. The recall affects 32,536 cases distributed nationwide with use-by dates between June 28, 2025 and January 28, 2026.
Product
Impossible Spicy Ground Sausage Meat from plants 14oz chub, UPC 8 16697 02109 5; 8 retail chubs per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0139-2025·2024-12-25
Primo Topical Anesthetic Gel Recalled for Manufacturing Defect
Primo Topical Anesthetic Gel (Benzocaine 20%) is recalled due to manufacturing defect. A Quality Unit inspection found scratches in the mixing vessel, causing inadvertent release of product that should have been rejected.
Product
Primo, Topical Anesthetic gel, Benzocaine 20%, Net Content: 1 oz. (30g), Gluten Free, Manufactured for: Primo Dental Products, 845 Third Avenue, 6th Floor, New York, NY 10022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0308-2025·2024-12-25
Bulk Food Ingredient Recalled for Potential Metal Contamination
Griffith Foods Ltd recalls bulk food ingredient Item 16354301 due to potential metal contamination. Product was distributed to food service facilities in Illinois, New York, North Carolina, Wisconsin, Texas, Tennessee, and Georgia.
Product
Item 16354301, MAXI - 44067705 - MAXI KR BA BA 3040 EX, 55.115 lb. bag
Category
Food
Distribution
7 states
HighFDA (Drugs)·D-0142-2025·2024-12-25
FDA Recalls Health-Tec Benzocaine Topical Anesthetic Due to Manufacturing Defect
Keystone Industries recalls Health-Tec Topical Anesthetic (Benzocaine 20%) lot BNZ-001646 due to manufacturing defects. Scratches found in the mixing vessel caused product rejection designation, but product was inadvertently shipped.
Product
HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0310-2025·2024-12-25
Bakestone Brothers Pita Bread Recalled Due to Metal Contamination
Bakestone Brothers Pita Bread is being recalled due to the presence of metal pieces in the product. Consumers who have purchased this bread should not consume it and should discard it.
Product
Bakestone Brothers Pita Bread, 6 Whole Wheat Pitas. Net Wt. 11.4 oz(325g) UPC 0 57391-01002 6. Manufactured by PBF pita Bread Factory Ltd, 8000 Winston Street, Burnaby British Columbia V5A 2H5. Product of Canada
Category
Food
Distribution
5 states
HighFDA (Food)·F-0305-2025·2024-12-25
Italian Meatball Dry Mix Recalled Due to Metal Contamination
GRIFFITH FOODS LTD is recalling 25,903 pounds of Italian Meatball Dry Mix due to potential metal pieces in the product. The product was distributed across IL, NY, NC, WI, TX, TN, and GA.
Product
Item 18968101, 100138 ITALIAN MBALL DRY MIX EX, 40.84 lb. bag
Category
Food
Distribution
7 states