State

Texas product recalls

72,936 recalls have nationwide distribution and so reach Texas. 12,389 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,389
Critical: 1,705
Severe: 2,407
Most recent: 2026-09-09

Of the 12,389 recalls naming Texas we have scored against our rubric, 1,705 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,407 (19%) are Severe.

Which agencies issued them

These figures cover only the 12,389 recalls whose distribution notice names Texas specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3026–3050 of 85325

HighFDA (Food)·H-0548-2026·2026-03-18
Vegetarian Chicken Flavor Ramen Express contains undeclared Yellow #5
Palmetto Gourmet Foods Inc. is recalling Vegetarian Chicken Flavor Ramen Express because the product contains undeclared Yellow #5 food coloring, a major allergen for some consumers.
Product
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Palm oil***" Contains: Wheat, Soy. UPC 8 10037 81004 2 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138
Category
Food
Distribution
32 states
HighFDA (Devices)·Z-1521-2026·2026-03-18
Link Endo-Model plateau 15-0027/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2026·2026-03-18
Link Endo-Model plateau 15-8030/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8030/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8030/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1530-2026·2026-03-18
GEM Premier 5000 PAK part 00055407510 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407510 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055407510.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1557-2026·2026-03-18
Vital Sync remote monitoring may not receive bedside monitor alarms
Covidien is recalling the HealthCast Vital Sync Remote Patient Monitoring System after complaints that alarms from the primary patient bedside monitor were not transmitted to or received by the remote system.
Product
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 /
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1497-2026·2026-03-18
IBA proton therapy system may not interrupt beam when gating fails
Ion Beam Applications is recalling PROTEUS 235 proton therapy systems because a disabled interface means the safety system may not interrupt beam delivery if the external gating signal is lost.
Product
IBA Proton Therapy System - PROTEUS 235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1536-2026·2026-03-18
GEM Premier 5000 part 00055415011 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No: 00055415011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2026·2026-03-18
Medline Medcrest surgical gowns may delaminate prematurely after recommended laundering
Medline is recalling Medcrest surgical gowns because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1524-2026·2026-03-18
GEM Premier 5000 PAK part 00055360004 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK, Part No. 00055360004.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1538-2026·2026-03-18
GEM Premier 5000 part 00055430008 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1541-2026·2026-03-18
GEM Premier 5000 part 00055445004 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055445004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055445004.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V162000·2026-03-18
Lexus NX, RX, and TX rearview camera software malfunction recall
Toyota is recalling certain 2022–2026 Lexus NX, RX, and TX vehicles because the rearview camera image may fail to display when the vehicle is in reverse, reducing rear visibility and increasing crash risk.
Product
LEXUS — LEXUS NX, RX, TX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1556-2026·2026-03-18
Artelon FlexBand Twist anchors failed bacterial endotoxin testing
International Life Sciences is recalling the Artelon FlexBand Twist .12, ref TW012, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1535-2026·2026-03-18
GEM Premier 5000 part 00055415010 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2026·2026-03-18
Link Endo-Model plateau 15-2835/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2835/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2835/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1537-2026·2026-03-18
GEM Premier 5000 part 00055430004 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430004.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1533-2026·2026-03-18
GEM Premier 5000 part 00055415005 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415005 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415005.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1549-2026·2026-03-18
Medartis APTUS 2.5 TriLock screw lots mixed with 2.8 mm
Medartis is recalling one lot of the APTUS 2.5 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.
Product
Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1560-2026·2026-03-18
Clearest Strep-A cassette test recalled because it lacks FDA clearance
Altruan GmbH is recalling the Clearest Strep-A Cassette Test, used to detect group A streptococci in throat swab samples, because the product is not cleared by the FDA.
Product
Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci (Strep A) in throat swab samples.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0547-2026·2026-03-18
Vegetarian Chicken Flavor Ramen recalled for undeclared Yellow #5
Palmetto Gourmet Foods is recalling VEGETARIAN CHICKEN FLAVOR RAMEN Express (3oz packages) because it contains undeclared Yellow #5, an FDA-approved food colorant that must be labeled for consumers with sensitivities.
Product
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Vegetable oil***" Contains: Wheat, Soy. UPC 8 10037 81061 5 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138
Category
Food
Distribution
32 states
ModerateFDA (Devices)·Z-1562-2026·2026-03-18
Chest drainage unit instructions updated to specify adult patient population
Medline is recalling three surgical kits containing Cardinal Health Aqua-Seal Chest Drainage Units because the instructions for use have been updated to clarify the target patient population as adults.
Product
Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model Number: DYNJ910851
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1559-2026·2026-03-18
Wondfo Streptococcal A self-test recalled because it lacks FDA clearance
Altruan GmbH is recalling the Wondfo Streptococcal A At-Home Self-Test, used for group A beta-hemolytic streptococcal infection, because the product is not cleared by the FDA.
Product
Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1550-2026·2026-03-18
Medartis APTUS TriLock screw lots mixed 2.5 mm and 2.8 mm
Medartis is recalling one lot of the APTUS 2.8 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.
Product
Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1561-2026·2026-03-18
Bisaf Strep A self-test recalled because it lacks FDA clearance
Altruan GmbH is recalling the Bisaf Strep A Self-Test, used to detect group A streptococcal antigens in throat swabs, because the product is not cleared by the FDA.
Product
Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal antigens in throat swabs.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1496-2026·2026-03-18
BD syringe batch may contain Luer Slip instead of Luer Lok
Becton Dickinson is recalling one lot of 10 mL Non-Sterile BD Luer-Lok Tip Syringes because some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Product
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Category
Medical Device
Distribution
Distributed nationwide