State

Texas product recalls

73,584 recalls have nationwide distribution and so reach Texas. 12,438 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,438
Critical: 1,716
Severe: 2,930
Most recent: 2026-10-21

Of the 12,438 recalls naming Texas we have scored against our rubric, 1,716 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,930 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

151–175 of 86022

SevereFDA (Drugs)·D-0023-2027·2026-10-14
FDA Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0085-2027·2026-10-14
Stryker Bard EP XT Decapolar Steerable Diagnostic EP Catheter Recalled for Sterile Barrier Breach
Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation.
Product
BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0017-2027·2026-10-14
biQ-FEL Beverage Recalled for Undeclared Sildenafil and Tadalafil
A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.
Product
biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA COLOMBIANA; Distributed by: Biofel
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0031-2027·2026-10-14
Carolina Infusion Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0021-2027·2026-10-14
FDA recalls injectable compounded mixture in single-use syringes
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
Product
QUAD-MIX( PAPAV/PHENTO/ALPROS/TROP) INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0015-2027·2026-10-14
Frozen Cheese Pie Recalled for Undeclared Milk Allergen
Queso Palmita GP LLC is recalling 20 packages of frozen Pastel de Queso (Cheese Pie) in Texas due to undeclared milk.
Product
QUESO PALMITA. Generic Name: Pastel de Queso (Cheese Pie). Intended use: Human consumption. Condition: Frozen. Shelf life or expected life: 90 days. Type of packaging: Vacuum, resealable package. Net weight: 1.2 lbs. UPC: 094922980045.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0078-2027·2026-10-14
Philips Spectral CT Systems Recalled for Software Issues Affecting Safety
Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.
Product
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model Numbers: 1. 728333 (U.S. and Outside U.S.), 2. 728340 (Outside U.S.), 3. 728344 (Outside U.S.), 4. 728345 (Outside U.S.);
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V674000·2026-10-14
PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Bunk Restraint Defect
PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.
Product
KENWORTH — KENWORTH, PETERBILT T680, W900, 579, 589
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0073-2027·2026-10-14
Steris VERIFY Dual Species Biological Indicator Recall for Spore Population Issues
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Product
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·N/A·2026-10-14
Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Product
Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0101-2027·2026-10-14
Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Product
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0090-2027·2026-10-14
Onkos My3D Personalized Pelvic Implant Recalled for Distribution Error
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Product
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0095-2027·2026-10-14
AVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination
AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.
Product
ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0103-2027·2026-10-14
AVID Medical Recalls Urology Kits for Potential Lubricant Contamination
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
Product
UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0082-2027·2026-10-14
DRG Sperm Ab ELISA Recalled for Potential False Negative Results
DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries.
Product
Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0013-2027·2026-10-14
Preferred Pharmaceuticals Recalls Lidocaine Ointment Due to Content Uniformity Failures
Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide.
Product
Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro Pharmaceuticals U.S.A., Inc., Prod# (NDC): 68788-7865-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0007-2027·2026-10-14
Mezzetta Golden Greek Peperoncini Recalled for Potential Mouse Contamination
G L Mezzetta Inc is recalling 32 fl oz jars of Golden Greek Peperoncini Medium Heat due to potential contamination with mice.
Product
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503 PRODUCT OF GREECE UPC: 073214003280
Category
Food
Distribution
22 states
ModerateFDA (Devices)·Z-0102-2027·2026-10-14
AVID Medical Recalls Heart Prep Trays for Lubricant Contamination
AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.
Product
HEART PREP TRAY; Model/Item Number (Kit): MECV97W;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0091-2027·2026-10-14
Onkos Surgical Recalls My3D Personalized Pelvic Implant Due to Distribution Error
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Product
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0014-2027·2026-10-14
Cipla Recalls Fosfomycin Tromethamine Due to Impurity Specification Failures
Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications.
Product
FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0077-2027·2026-10-14
Halyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
GRI Medical is recalling Halyard Laparoscopy Comprehensive Pack II kits because they contain a latex urethral catheter despite being labeled as latex-free.
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0100-2027·2026-10-14
AVID Medical Recalls Plastic Trays Due to Lubricant Contamination
AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.
Product
PLASTICS TRAY; Model/Item Number (Kit): EURO053;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0083-2027·2026-10-14
Beckman Coulter Recalls DxC 500i Clinical Analyzer Modules Due to Software Error
Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules because a software issue can cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.
Product
DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No. C63522 2. DxC 500 AU Module, DxC 500i, Part No. C63521 3. Access 2 Module, DxC 500i, Part No. C13252
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0097-2027·2026-10-14
Avid Medical Recalls Open Heart Kits Due to Lubricant Contamination
Avid Medical is recalling 124 Open Heart CFH kits because they may be contaminated with a lubricant used during manufacturing.
Product
PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0092-2027·2026-10-14
Avid Medical Recalls Davinci Trucustom Bundles Due to Lubricant Contamination
Avid Medical, Inc. is recalling 144 Davinci Trucustom Bundles because they may be contaminated with a lubricant used during manufacturing.
Product
DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
Category
Medical Device
Distribution
Distributed nationwide