State

Texas product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25976–26000 of 85946

HighFDA (Devices)·Z-0274-2022·2021-12-01
Freelite Human Lambda Free Kit Recalled for Calibration Curve Inaccuracy
The Binding Site Group recalled 2,254 Freelite Human Lambda Free Kits due to calibration curve issues that may produce higher-than-expected activity readings and affect measurement accuracy.
Product
Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S
Category
Medical Device
Distribution
13 states
HighNHTSA·21V935000·2021-12-01
Audi Recalls 2022 E-Tron GT Vehicles Due to Air Suspension Defect
Volkswagen Group of America is recalling 2022 Audi E-Tron GT vehicles because a loose retaining ring on air suspension struts may compromise handling and increase crash risk.
Product
AUDI — AUDI E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0295-2022·2021-12-01
Medtronic Wireless Recharger Model WR9200 Becomes Unresponsive on Improper Use
Medtronic is recalling the Wireless Recharger Model WR9200 used with RestoreUltra and RestoreSensor neurostimulator implants. The recharger becomes unresponsive if charging instructions from the user guide are not followed correctly.
Product
Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor (Model 37714), Restore Ultra SureScan MRI (Model 97712), and RestoreSensor SureScan MRI (Model 97714) implantable neurostimulators.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0283-2022·2021-12-01
CT Scanner Software Issue May Interrupt Diagnostic Workflows and Delay Diagnoses
Siemens SOMATOM Force CT scanners with software syngo.CT VB20 may experience workflow interruptions, causing diagnosis delays and requiring additional patient scans and contrast media. No illnesses or injuries have been reported.
Product
SOMATOM Force with software syngo.CT VB20 Model #10742326
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0284-2022·2021-12-01
CT Scanner Software Issue Causes Workflow Interruptions and Diagnostic Delays
A software issue in SOMATOM Definition AS CT scanners may cause workflow interruptions, leading to diagnostic delays and the need for patient rescans. The recall affects approximately 665 units distributed nationwide.
Product
SOMATOM Definition AS with software syngo.CT VB20 Model #8098027
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0240-2022·2021-12-01
Medical X-Ray Systems Missing Required Radiation Warning Labels
Philips Healthcare is recalling ProxiDiagnost N90 diagnostic X-ray systems that lack required FDA radiation warning labels. Some units nationwide were found missing the mandatory radiation safety labels and certification statements required by federal standards.
Product
ProxiDiagnost N90 is multi-functional general R/F systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0303-2022·2021-12-01
Siemens Artis Q.zen Angiography System May Fail to Fire X-rays During Simultaneous Operations
Three Siemens Artis Q.zen angiography systems may fail to fire X-rays when the source-to-image distance lift is activated simultaneously with X-ray commands. This causes a procedural delay.
Product
Artis Q.zen floor with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848353
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0298-2022·2021-12-01
Siemens Artis Zee Angiography System Software May Prevent X-Ray Activation
Siemens is recalling 19 units of its Artis zee angiography system due to a software issue that may prevent x-ray activation under specific operating conditions, causing procedural delay.
Product
Artis zee multi-purpose with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094139
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0297-2022·2021-12-01
Siemens Artis zee x-ray system may delay imaging delivery during procedures
Siemens is recalling Artis zee ceiling-mounted x-ray imaging systems equipped with VD12 software. A software issue may prevent x-ray delivery when the source-to-image distance lift is activated during procedures, resulting in procedural delays.
Product
Artis zee ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number:10094137
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0275-2022·2021-12-01
da Vinci Surgical Drapes Recalled for Incorrect Expiration Date on Packaging
Intuitive Surgical recalls 1,740 da Vinci Instrument Arm Drapes due to incorrect expiration dates on package labeling. The error may prevent accurate verification of sterility assurance dates.
Product
The da Vinci Xi and X surgical systems (IS4000 and IS4200) each consist of three main components: the Surgeon Console (SC), the Vision Cart (VC), and the Patient Cart (PC). The Patient Cart is the operative component of the system and its primary function is to support the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0258-2022·2021-12-01
Diclofenac Sodium Topical Solution recalled for defective container
Teligent Pharma, Inc. is recalling Diclofenac Sodium Topical Solution USP 1.5% w/w due to a defective container. The recall affects approximately 2,664 bottles distributed nationwide.
Product
Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL) plastic bottles, Rx only, Teligent Pharma, Inc., Buena, New Jersey, 08310, NDC 52565-002-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0259-2022·2021-12-01
Diclofenac Sodium Topical Solution recalled for defective container
Teligent Pharma, Inc. is recalling Diclofenac Sodium Topical Solution USP 1.5% due to a defective container. The recall affects 5,400 units distributed nationwide.
Product
Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL) plastic bottles, Rx only, Teligent Pharma, Inc., Buena, New Jersey, 08310, NDC 70512-025-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0296-2022·2021-12-01
Medical Imaging System May Fail to Release X-rays Under Specific Conditions
Siemens Artis zee floor angiography systems may fail to release x-rays when the SID lift and x-ray functions are activated simultaneously, causing procedural delay. Three units are affected.
Product
Artis zee floor with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094135
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0305-2022·2021-12-01
Siemens Artis Q.zen Angiography System X-Ray Imaging Delay Issue
Siemens has recalled two Artis Q.zen angiography systems due to a software issue that may prevent x-ray imaging and delay procedures when SID lift and x-ray controls are activated simultaneously.
Product
Artis Q.zen biplane with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number:10848355
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0299-2022·2021-12-01
Siemens Artis Zee Biplane X-ray Imaging System Software Malfunction
Siemens Artis zee biplane X-ray imaging systems may fail to release X-rays when the source-to-image distance lift is activated simultaneously, resulting in procedural delays.
Product
Artis zee biplane with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094141
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0302-2022·2021-12-01
Siemens Artis Q Biplane X-ray System Software Imaging Delay Issue
Siemens Medical Solutions is recalling 15 Artis Q biplane diagnostic x-ray systems due to a software issue in the VD12-angiography subsystem. When source-to-image distance lift is activated simultaneously with x-ray release, the system fails to activate and displays an error message, causing procedural delay.
Product
Artis Q biplane with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848282
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0300-2022·2021-12-01
Siemens Artis Q floor angiography system: X-ray failure during SID lift operation
Siemens Artis Q floor angiography systems may fail to produce x-ray when SID lift movement is activated during x-ray release, resulting in procedural delays. The system displays an error message.
Product
Artis Q floor with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848280
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0304-2022·2021-12-01
Siemens Artis Q.zen Angiography System X-ray Activation Failure
Siemens is recalling 15 Artis Q.zen angiography systems that may fail to generate x-rays when the lift mechanism and x-ray release are activated simultaneously, potentially causing a procedural delay.
Product
Artis Q.zen ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848354
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0263-2022·2021-12-01
Carvedilol Tablets Recalled for Failed Impurities and Degradation Specifications
Aurobindo Pharma USA Inc. is recalling Carvedilol 6.25 mg tablets nationwide due to failed impurities and degradation specifications. Affected containers bear Batch QG0619030-A with expiration date 11/2022.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0255-2022·2021-12-01
Topiramate 50 mg tablets recalled due to discoloration
Unichem Pharmaceuticals USA Inc is recalling Topiramate 50 mg tablets nationwide due to discoloration. The affected lot is ZTPM20044, expiring 09/30/2022.
Product
TOPIRAMATE — TOPIRAMATE (TOPIRAMATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0257-2022·2021-12-01
Butalbital, APAP, Caffeine Tablets Missing Schedule III Label
Bryant Ranch Prepack is recalling Butalbital, APAP, Caffeine 50/325/40 mg tablets in multiple bottle sizes because the controlled substance classification "CIII" is missing from the label.
Product
Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode 083929164865; b) 20-count bottles, NDC: 71335-1767-01, barcode 083921157837; c) 30-count bottles, NDC: 71335-1767-02, barcode 083922165687, d) 60-count bottles, NDC…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0256-2022·2021-12-01
Butalbital/APAP/Caf Tablets Missing Controlled Substance Label
Bryant Ranch Prepack is recalling Butalbital, APAP, and Caffeine 50/325/40 mg tablets because the label is missing the controlled substance classification "CIII" required by law.
Product
Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b) 60-count bottles, NDC: 63629-8392-03, barcode 083923152614; c) 90-count bottles, NDC:63629-8392-04, barcode 083924152614, Lannett Company Inc; Rx only, Packaged…
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21T018000·2021-11-30
Sailun Recalls Specific Tires Due to Belt Separation Risk
Sailun is recalling specific ST235/80R16 and ST235/85R16 tires due to a manufacturing issue that may cause belt separation. This defect could lead to loss of vehicle control and increase crash risk.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E097000·2021-11-30
Tenneco Recalls MOOG and NAPA Tie Rods Due to Heat Treatment Defect
Tenneco Automotive is recalling specific MOOG and NAPA tie rods that may not have been heat-treated properly. This defect can cause tie rod failure and loss of steering control.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E098000·2021-11-30
Meritor Recalls 180 Series Drive Pinions Due to Fracture Risk
Meritor is recalling 180 Series Drive Pinions because they may fracture and engage the parking brake without warning, increasing crash risk.
Product
POWER TRAIN:AXLE ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide