State

Texas product recalls

73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24051–24075 of 85923

HighFDA (Devices)·Z-0913-2022·2022-04-20
Hammertoe Correction Surgical System Recalled for Driver Connection Defect
Nextremity Solutions recalls the Nextra Hammertoe Correction System because the driver's proximal end is oversized, making it difficult to connect and remove from the implant, potentially delaying surgery.
Product
Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut SKU: NX-3532K-SC Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0989-2022·2022-04-20
Cinnamon Crumb Cake Recalled for Potential Foreign Materials
Continental Mills voluntarily recalls Krusteaz Cinnamon Crumb Cake (Lot KX2063) due to potential foreign materials that could pose a choking or injury risk.
Product
Item # 722-0105, Krusteaz Cinnamon Crumb Cake. Product is shelf stable and packaged in a box. net wt. 21 oz., UPC 0 41449 11140 7.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0937-2022·2022-04-20
CLARAVUE Pre-wired Electrode fails to meet electrical safety specification
Graphic Controls' CLARAVUE Pre-wired Electrode units fail to meet electrical safety specifications required for defibrillation. The device delivers an inefficient electrical charge and may result in ineffective defibrillation.
Product
CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778 50601-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0929-2022·2022-04-20
Siemens Atellica CH Hemoglobin A1c Reagent Kits Recalled for Quality Control Issues
Siemens Healthcare is recalling Atellica CH Hemoglobin A1c reagent kits due to potential reagent carryover affecting quality control and patient test results. The issue may cause inaccurate diabetes monitoring measurements.
Product
Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H), Siemens Material Number 11097536
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2022·2022-04-20
Nextra Hammertoe Correction System surgical instruments recalled for defective connector
Nextremity Solutions recalls 459 units of the Nextra Hammertoe Correction System due to an oversized proximal driver end that prevents proper connection and removal during surgery.
Product
Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU: NX-4532K-SC Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0984-2022·2022-04-20
Great Value Buttermilk Pancake Mix Recalled for Foreign Materials
Continental Mills is recalling Great Value Buttermilk Pancake & Waffle Mix (item #714-5000) due to foreign materials. Approximately 1,125 cases were distributed nationwide.
Product
Item # 714-5000, Great Value Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 32 oz., UPC 0 78742 37082 8.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0766-2022·2022-04-20
Cyanocobalamin Injection Recalled for Subpotent Drug - Out of Specification Assay
Aurobindo Pharma USA Inc. is recalling 433,809 vials of Cyanocobalamin injection nationwide because assay testing showed the drug is subpotent, containing less than the specified 1,000 mcg/mL of active ingredient. Affected lots with specific expiration dates from September 2022 to April 2023 are identified for recall.
Product
CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0926-2022·2022-04-20
Philips Autoclavable Temperature Probes: Updated Cleaning Instructions
Philips is updating instructions for cleaning and disinfecting reusable autoclavable temperature probes due to revisions needed in the disinfection process.
Product
The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s: 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1000-2022·2022-04-20
Dietary Supplement Recalled for Undeclared New Ingredient
Bio-Botanica is recalling NATURE's ANSWER Coral Calcium supplements because the product contained cesium chloride, a New Dietary Ingredient. The recall affects 6852 bottles distributed to 17 states.
Product
NATURE's ANSWER Coral Calcium; Antioxidant Benefits*; 1000mg Coral Calcium per serving; DIETARY SUPPLEMENT; 90 capsules
Category
Drug
Distribution
17 states
ModerateFDA (Food)·F-0988-2022·2022-04-20
Krusteaz Belgian Waffle Mix recalled due to foreign materials contamination
Continental Mills voluntarily recalled 450 cases of Krusteaz Belgian Waffle Mix nationwide due to the presence of foreign materials.
Product
Item # 721-1000, Krusteaz Belgian Waffle Mix. Product is shelf stable and packaged in a box. net wt. 28 oz., UPC 0 41449 00186 9.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0933-2022·2022-04-20
Medical Device Linearity Standards Recalled Due to Improper Storage Controls
Medline Industries is recalling Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards due to improper storage controls that may affect test result timing. The recall affects 10 boxes distributed to healthcare facilities in six states.
Product
Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards, packaged in boxes containing Levels 1-6, 1 x 4 mL each, REF 2450-604, Medline catalog number S-O2450604, IVD.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-0930-2022·2022-04-20
Siemens Atellica CH Fructosamine Reagent Recalled for Potential Carryover
Siemens Healthcare Diagnostics is recalling Atellica CH Fructosamine reagent (lots 211359, 211451) due to potential reagent carryover that could affect diagnostic test accuracy.
Product
Atellica CH Fructosamine (Fruc), Siemens Material Number 11097637
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0917-2022·2022-04-20
FDA Recalls Touch Screen Modules for IVUS Imaging Systems
Volcano Corp is recalling MM-TSM touch screen modules used with IntraSight Integrated IVUS systems because they may crack or become damaged, potentially rendering the imaging equipment non-functional.
Product
MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller), Part Numbers: 300002018101, 300002018102, used with IntraSight Integrated (Part Number: 797403) IVUS systems
Category
Medical Device
Distribution
50 states
LowFDA (Devices)·Z-0901-2022·2022-04-20
IntraSight Mobile IVUS touch screen modules missing required labeling information
IntraSight Mobile IVUS Systems touch screen modules lack required labeling information including device identifier and manufacturer information. Affected units were distributed to healthcare facilities in the US and internationally.
Product
IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102
Category
Medical Device
Distribution
15 states
HighNHTSA·22E034000·2022-04-19
Enerco Recalls LP Gas Quick Connector Fittings for Fire Risk
Enerco is recalling specific Mr. Heater LP gas quick connector fittings because they may crack and leak gas, increasing the risk of fire.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:LINES AND FITTINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V265000·2022-04-19
Maserati Recalls 2022 MC20 Vehicles Due to Brake Light Malfunction
Maserati is recalling 2022 MC20 vehicles because faulty rear tail lights may cause brake lights to flicker, potentially confusing other drivers and increasing crash risk.
Product
MASERATI — MASERATI MC20
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·22V266000·2022-04-19
Triple E RV Recalls 2021-2022 Wonder W24RL for Incorrect Weight Decal
Triple E Recreational Vehicles is recalling 2021-2022 Wonder W24RL models because an incorrect weight decal may lead to overloading the storage compartment.
Product
TRIPLE E RV — TRIPLE E RV WONDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V264000·2022-04-18
2022 Tesla Model X: Missing Seat Reinforcement Bracket Safety Defect
Tesla is recalling one 2022 Model X vehicle due to a missing body structure reinforcement bracket at the second-row seat. This failure to comply with federal seat restraint standards increases the risk of occupant injury in a crash.
Product
TESLA — TESLA MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V263000·2022-04-18
Tesla Model 3 Speedometer Unit Display May Fail in Track Mode
Tesla is recalling certain 2018-2022 Model 3 Performance vehicles because the speedometer's mph/km/h unit display may fail in Track Mode. Drivers may not know their vehicle's speed, increasing crash risk. Tesla will provide a free software update.
Product
TESLA — TESLA MODEL 3
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·009-2022·2022-04-16
Firehouse Jams Recalls Uncured Bacon Marmalade Produced Without Inspection
Firehouse Jams is recalling 3,819 pounds of uncured bacon marmalade produced without federal inspection. No adverse reactions have been reported.
Product
Firehouse Jams, LLC Recalls Uncured Bacon Marmalade Products Produced Without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22V260000·2022-04-15
Rugged Mountain Custom RV Travel Trailer Recall for Coupler Welding Defect
Tiny Idahomes is recalling 2021-2022 Rugged Mountain Custom RV Travel trailers because an improperly welded coupler may cause the trailer to separate from the tow vehicle.
Product
RUGGED MOUNTAIN CUSTOM RV — RUGGED MOUNTAIN CUSTOM RV TRAVEL TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V262000·2022-04-15
2019-2021 Autocar Xpeditor Vehicles Recall: Inoperable Hazard Lights
Autocar is recalling 2019-2021 Xpeditor vehicles because the hazard lights do not function when the ignition is off, increasing crash risk. Dealers will repair or replace the wire harness at no charge.
Product
AUTOCAR — AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V261000·2022-04-15
2021 Mercedes-Benz AMG GLC63 S Headlight Failure Recall
Mercedes-Benz is recalling certain 2021 GLC models because the headlight electrical connection may not be watertight, risking headlight failure. Reduced visibility increases crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63 S, AMG GLC63, AMG GLC43, GLC 300
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V246000·2022-04-14
GM Recalls 2015 Enclave, Traverse, Acadia for Air Bag Defect
General Motors is recalling 2015 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because the driver's air bag inflator may explode during deployment.
Product
GMC — GMC, BUICK, CHEVROLET ACADIA, ENCLAVE, TRAVERSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V257000·2022-04-14
Bentley Recalls 2021-2022 Bentayga Vehicles Due to Unlocked Second Row Seats
Bentley is recalling 2021-2022 Bentayga vehicles because second row seats may not be locked on all rails, increasing injury risk in a crash.
Product
BENTLEY — BENTLEY BENTAYGA
Category
Vehicle
Distribution
Distributed nationwide