State

Texas product recalls

72,820 recalls have nationwide distribution and so reach Texas. 12,385 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,385
Critical: 1,703
Severe: 2,405
Most recent: 2026-09-06

Of the 12,385 recalls naming Texas we have scored against our rubric, 1,703 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (19%) are Severe.

Which agencies issued them

These figures cover only the 12,385 recalls whose distribution notice names Texas specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

676–700 of 85205

HighFDA (Food)·H-1154-2026·2026-07-22
Pillsbury Bread Rolls Hard Roll Dough Recalled for Glass
General Mills is recalling Pillsbury Bread Rolls Hard Roll Dough due to potential glass contamination. Affected products were distributed across multiple states.
Product
Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-2718-2026·2026-07-22
Olympus Toomey Evacuator 30cc medical device sterilization parameters recalled
Olympus Corporation recalled the Toomey Evacuator 30cc with Adaptor (Model 188) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
Product
Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2730-2026·2026-07-22
Orthofix MINIRAIL external fixation devices recalled for incorrect labeling
Orthofix U.S. LLC is recalling 19 units of Orthofix MINIRAIL orthopedic external fixation devices distributed across the US due to incorrect model labeling that could lead to surgical use of the wrong device.
Product
Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-2741-2026·2026-07-22
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
Maquet Cardiovascular is recalling Vasoview Hemopro 2 devices from Lot 3000547797 due to exposure to out-of-specification sterilization during gamma sterilization. The affected devices may not be properly sterilized.
Product
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2726-2026·2026-07-22
GE Medical Optima XR200/220/240amx Mobile Radiographic Systems Recall
GE HealthCare recalls certain Optima XR200/220/240amx mobile radiographic systems where safety testing may have been incomplete after column replacement. A failed counterpoise cable could cause the X-ray arm to drop on patients.
Product
Optima XR200amx, Mobile Digital-Ready Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2727-2026·2026-07-22
GE Optima XR200/220/240amx Radiographic System Column Safety Mechanism
GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.
Product
Optima XR220amx, Mobile Digital-Ready Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2728-2026·2026-07-22
Mobile Digital Radiographic System Arm Drop Risk During Patient Exams
GE HealthCare is recalling certain Optima XR200/220/240amx Mobile Digital Radiographic Systems due to potential failure of the Column Safety mechanism, which could cause the X-ray arm to drop during patient exams. The issue stems from incomplete functional testing of the safety pawl after column replacement.
Product
Optima XR240amx, Mobile Digital Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V473000·2026-07-22
2024–2026 Volkswagen Atlas and Atlas Cross Sport Rearview Camera Software
Volkswagen is recalling 2024–2026 Atlas and Atlas Cross Sport vehicles due to a low-voltage electrical event that may cause the rearview camera display to fail, reducing rear visibility.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2725-2026·2026-07-22
Rapid Refill Continuous Injection System Recalled for Syringe Loosening Risk
Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.
Product
Rapid Refill Continuous Injection System, UPN M00566001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1175-2026·2026-07-22
OLA-OLA Pounded Groundnuts recalled for undeclared peanuts
Fayus Inc. is voluntarily recalling OLA-OLA Pounded Groundnuts because the product contains undeclared peanuts, a major allergen, which poses a risk to consumers with peanut allergies.
Product
OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods Sacramento, CA 95828 Product of USA INGREDIENTS: Pounded Groundnuts (Intwilo) UPC: 650655764330
Category
Food
Distribution
1 state
HighNHTSA·26V475000·2026-07-22
Freightliner Trucks Recalled for Low Beam Headlight Software Error
Daimler Trucks North America is recalling 2026-2027 Freightliner models because a software error may cause low beam headlights to illuminate improperly, increasing crash risk.
Product
FCCC — FCCC, FREIGHTLINER S2C, S2RV, BUSINESS CLASS M2, EM2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-1156-2026·2026-07-22
Winfield's CWB Chocolate Bars Recalled for Undeclared Milk Allergen
Chocolate Bar Holdings LLC is recalling Winfield's CWB Chocolate Bars in multiple shapes and sizes due to undeclared milk allergen. Consumers with milk allergies should not consume these products.
Product
Winfield's CWB Chocolate Bar, packed in clear cello bag with fabric bow on top. Manufactured by CBSL Commissary (DBA Winfield's Chocolate Bar) 9127 Stella Link Rd Houston Texas. Multiple product shapes/sizes: 1) Cat, Net wt. 8oz (226.8g), UPC: 00810079833030, Unit size 5 x 3 1/
Category
Food
Distribution
1 state
HighNHTSA·26V472000·2026-07-22
Coach and Equipment Recalls Phoenix and Metrolite Buses with Lift Defect
Coach and Equipment is recalling 2024-2026 Phoenix and Metrolite buses because a wheelchair lift may fail to stop, increasing injury risk.
Product
COACH AND EQUIPMENT — COACH AND EQUIPMENT METROLITE, PHOENIX
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2734-2026·2026-07-22
Papablic Replacement Brush Heads Recalled Due to Breakage Risk
Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.
Product
Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0685-2026·2026-07-22
Leader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
Bell Pharmaceuticals is recalling Leader Carbamide Peroxide 6.5% Earwax Removal Kit due to subpotency—the active ingredient is significantly reduced (approximately 0.6% versus the expected 6–7%) and the pH is low.
Product
LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB — LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2731-2026·2026-07-22
Orthofix Articulated Minirail Fixator devices recalled for incorrect labeling
Orthofix U.S. LLC is recalling Articulated Minirail Fixator external fixation devices due to incorrect model labeling. Three models were mislabeled: M101 labeled as M103, M103 labeled as M101, and M122 labeled as M111.
Product
Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111, Unilateral orthopedic/trauma external fixation device
Category
Medical Device
Distribution
26 states
ModerateFDA (Drugs)·D-0684-2026·2026-07-22
Good Neighbor Pharmacy Earwax Removal Drug Recalled for Low Potency
Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.
Product
GOOD NEIGHBOR PHARMACY EARWAX REMOVAL — GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2744-2026·2026-07-22
Photera 600 3-D phototherapy device UV sensor calibration error recall
Daavlin Distributing Company is recalling Photera 600 3-D phototherapy devices because the UV sensor gain calculation is incorrect, causing inaccurate ultraviolet output measurement.
Product
Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0687-2026·2026-07-22
Meijer Earwax Removal Kit Recalled for Subpotent Active Ingredient
Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.
Product
MEIJER EARWAX REMOVAL KIT — MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0688-2026·2026-07-22
CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient
CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.
Product
CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2722-2026·2026-07-22
da Vinci SP Instrument Arm Drape may detach during surgical procedures
Intuitive Surgical is recalling da Vinci SP Instrument Arm Drapes because the drape rings may detach, exposing the instrument arm and potentially delaying procedures. The recall affects 11,113 units distributed worldwide.
Product
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2733-2026·2026-07-22
Papablic Replacement Brush Heads Recalled for Potential Breakage
Papablic Inc is recalling certain Papablic18B replacement brush head packs because the brush heads may break during use.
Product
Papablic Replacement Brush Heads. Model Number: Papablic18B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0680-2026·2026-07-22
Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.
Product
QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1152-2026·2026-07-22
Liquid Hope Organic Meal Replacement Formula Subpotent Vitamin A Recall
Nutricia North America is recalling Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley because the product contains less vitamin A than labeled. A testing laboratory used an incorrect method that overstated the vitamin A concentration.
Product
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2
Category
Food
Distribution
49 states
ModerateFDA (Devices)·Z-2737-2026·2026-07-22
Medline Kits with Zimmer Biomet Mixing Bowls and Spatulas Recalled
Medline Industries is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal defects that risk sterility breach during surgical procedures.
Product
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
Category
Medical Device
Distribution
Distributed nationwide