State

Texas product recalls

72,986 recalls have nationwide distribution and so reach Texas. 12,390 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,390
Critical: 1,705
Severe: 2,407
Most recent: 2026-09-16

Of the 12,390 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 12,390 recalls whose distribution notice names Texas specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7376–7400 of 85376

SevereFDA (Devices)·Z-1702-2025·2025-05-07
Tibial Augment devices recalled for missing screw thread
Waldemar Link GmbH & Co. KG is recalling Tibial Augment devices distributed nationwide because preassembled Femoral Augment screws were delivered missing their threads.
Product
Tibial Augment; Item Numbers: (1) 880-331/11 (Sz. 1-2 - cemented x-sm), (2) 880-331/12 (Sz. 1-2 - cemented sm), (3) 880-331/13 (Sz. 1-2 - cemented md), (4) 880-331/21 (Sz. 1-2 - cemented lg), (5) 880-331/22 (Sz. 1-2 - cemented x-lg), (6) 880-331/23 (Sz. 1-2 - cemented xx-lg), (7)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1632-2025·2025-05-07
GE Healthcare CARESTATION 650C A1 Anesthesia System Ventilation Recall
GE Healthcare CARESTATION 650C A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Ventilation can be achieved using alternate modes or manual ventilation.
Product
GE Healthcare CARESTATION 650C A1, Model/REF Number 1012-9655-000. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1624-2025·2025-05-07
GE Healthcare CARESTATION anesthesia systems ventilation malfunction recall
GE Healthcare CARESTATION 620 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Effective ventilation is available in Pressure Control or Manual ventilation modes.
Product
GE Healthcare CARESTATION 620 A1, Model/REF Number 1012-9620-000. anesthesia systems
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1704-2025·2025-05-07
Enhanced Verify Evaluation Handset May Fail to Connect to Neurostimulator
Medtronic Enhanced Verify Evaluation Handsets (CFN HH90130FA) may fail to communicate with neurostimulators due to faster processing speed, causing therapy to stop and patients to experience return of underlying symptoms.
Product
Enhanced Verify Evaluation Handset (CFN HH90130FA)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1695-2025·2025-05-07
Quantum Informatics VIPER Physiological Monitor Recalled for Lack of FDA Clearance
Spectrum Medical Ltd. is recalling the Quantum Informatics VIPER, a patient monitoring software device, because it was marketed without required FDA clearance. The software is used in operating rooms to provide patient safety information.
Product
Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product Description: VIPER is a software-only device (SaMD) that is intended to provide near real-time patient safety and clinical best practice soluti
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-1626-2025·2025-05-07
GE Healthcare Carestation 620 SE Anesthesia System Ventilation Defect Recall
GE Healthcare is recalling certain Carestation 620 SE anesthesia systems (27 units) because they may not provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes remain functional.
Product
GE Healthcare Carestation 620 SE, Model/REF Number 1012-9620-012. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1635-2025·2025-05-07
GE Healthcare CARESTATION 750 Anesthesia System Volume Control Ventilation Failure
Certain GE Healthcare CARESTATION 750 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Affected systems can deliver ventilation through alternative modes or manual ventilation.
Product
GE Healthcare CARESTATION 750 A1, Model/REF Number 1012-9750-000. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1696-2025·2025-05-07
Quantum Informatics VISION LIVE VUE Patient Monitor Recalled Without FDA Clearance
Spectrum Medical Ltd. is recalling the Quantum Informatics VISION / LIVE VUE patient monitoring software because it was marketed without required FDA clearance or approval.
Product
Brand Name: Quantum Informatics - VISION / LIVE VUE Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product Description: VISION / LIVE VUE is a software-only device (SaMD) that is intended to provide near real-time patient safety and clini
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-1638-2025·2025-05-07
GE Healthcare CARESTATION Anesthesia Systems may not ventilate properly
GE Healthcare is recalling certain CARESTATION anesthesia systems that may fail to provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes remain functional.
Product
GE Healthcare CARESTATION 750c A2, Model/REF Number 1012-9755-002. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1634-2025·2025-05-07
GE Healthcare Carestation 650c A1 Anesthesia System Ventilation Failure
GE Healthcare is recalling certain Carestation 650c A1 anesthesia systems worldwide because they may not provide effective ventilation in Volume Control Ventilation mode, limiting patient ventilation options during anesthesia delivery.
Product
GE Healthcare Carestation 650c A1, Model/REF Number 1012-9655-200. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1633-2025·2025-05-07
GE Healthcare CARESTATION Anesthesia Systems Volume Control Ventilation Failure
GE Healthcare CARESTATION anesthesia delivery systems may fail to provide effective ventilation in Volume Control Ventilation mode. Affected units can deliver ventilation through Pressure Control Ventilation modes or manual ventilation.
Product
GE Healthcare CARESTATION 650C A2, Model/REF Number 1012-9655-002. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1700-2025·2025-05-07
Posterior Femoral Augment with Missing Screw Thread Recalled
Waldemar Link is recalling Posterior Femoral Augments used in knee surgery because some units were delivered with a preassembled screw missing its thread, which could compromise surgical fixation.
Product
Posterior Femoral Augment; Item Numbers: (1) 880-310/11 (Sz. 0 - cemented sm), (2) 880-310/21 (Sz. 0 - cemented lg), (3) 880-311/11 (Sz. 1-2 - cemented sm), (4) 880-311/21 (Sz. 1-2 - cemented lg), (5) 880-313/11 (Sz. 3-4 - cemented sm), (6) 880-313/12 (Sz. 3-4 - cemented md), (7)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1628-2025·2025-05-07
GE Healthcare Carestation 650 A1 Anesthesia System Ventilation
Certain GE Healthcare Carestation 650 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes or manual ventilation can be used.
Product
GE Healthcare CARESTATION 650 A1, Model/REF Number 1012-9650-000. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1636-2025·2025-05-07
GE Healthcare CARESTATION Anesthesia Systems Ventilation Mode Failure Recall
Certain GE Healthcare CARESTATION 750 A2 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Users should switch to Pressure Control Ventilation or Manual ventilation modes.
Product
GE Healthcare CARESTATION 750 A2, Model/REF Number 1012-9750-002. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1627-2025·2025-05-07
GE Healthcare Anesthesia Systems Recalled Over Ventilation Failure
GE Healthcare is recalling certain Carestation 620/650/650c and 750/750c anesthesia delivery systems because they may not provide effective ventilation in Volume Control Ventilation (VCV) mode. The issue does not affect Pressure Control Ventilation (PCV), PCV-VG, or manual ventilation modes.
Product
GE Healthcare Carestation 620 A1, Model/REF Number 1012-9620-200. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0398-2025·2025-05-07
Nicardipine Hydrochloride Injection Recalled for Potential Sterility Issues
American Regent, Inc. is recalling Nicardipine Hydrochloride Injection due to product leakage around the vial neck that could compromise sterility assurance. The recall affects multiple lots distributed nationwide.
Product
NICARDIPINE HYDROCHLORIDE — NICARDIPINE HYDROCHLORIDE (NICARDIPINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1629-2025·2025-05-07
GE Healthcare CARESTATION anesthesia systems may not ventilate effectively
Certain GE Healthcare CARESTATION 620, 650, 650c, 750, and 750c anesthesia delivery systems may not provide effective ventilation in Volume Control Ventilation (VCV) mode. Effective ventilation is available using other ventilation modes or manual ventilation.
Product
GE Healthcare CARESTATION 650 A2, Model/REF Number 1012-9650-002. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1625-2025·2025-05-07
GE Healthcare CARESTATION 620 A2 Anesthesia System Ventilation Failure
Certain GE Healthcare CARESTATION anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation (VCV) mode. Alternative ventilation modes or manual ventilation can be used.
Product
GE Healthcare CARESTATION 620 A2, Model/REF Number 1012-9620-002. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1631-2025·2025-05-07
GE Healthcare Carestation Anesthesia Systems Ventilation Defect Recall
Certain GE Healthcare Carestation anesthesia delivery systems may fail to provide effective ventilation in Volume Control Ventilation (VCV) mode. Affected systems can still be used safely in Pressure Control Ventilation or Manual ventilation modes.
Product
GE Healthcare Carestation 650 A1, Model/REF Number 1012-9650-200. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1701-2025·2025-05-07
L-Shaped Femoral Augment with Missing Screw Thread
Waldemar Link GmbH & Co. KG is recalling L-Shaped Femoral Augments because the preassembled femoral augment screw was missing its thread. The defect could affect the device's structural integrity during orthopedic surgery.
Product
L-Shaped Femoral Augment; Item Numbers: (1) 880-320/12 (Sz. 0 - cemented sm), (2) 880-320/22 (Sz. 0 - cemented lg), (3) 880-321/12 (Sz. 1-2 - cemented sm), (4) 880-321/22 (Sz. 1-2 - cemented lg), (5) 880-323/13 (Sz. 3-4 - cemented sm), (6) 880-323/23 (Sz. 3-4 - cemented lg), (7)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2025·2025-05-07
Belmont 3.0 Liter Disposable Set Recalled for Cracked Female Connector
Belmont Instrument LLC is recalling the 3.0 Liter Disposable Set (Model 903-00032) due to a potential crack in the female connector on the Heat Exchanger/patient line set that can cause fluid leaks during device priming.
Product
3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The P/N 903-00032 consists of 4 Large Volume Reservoirs (P/N 903-00018) and 4 Heat Exchanger/Patient Line set (P/N 403-00382). The two components are packaged separately in individual pouches and placed in the
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0748-2025·2025-05-07
Cookie Butter Banana Pie recalled for undeclared almond allergen
Dianne's Fine Desserts is recalling Cookie Butter Banana Pie due to undeclared almonds. Consumers with almond allergies face risk of allergic reaction.
Product
Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained inside: "Cookie Butter Banana Pie" NET WT. 11 LB 2.8 OZ (5.06 kg) GROSS WT: 12.96 LB (5.88 kg)
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-1714-2025·2025-05-07
Medline Sterile Water and Saline Bottles Leaking at Seal Interface
Medline is recalling sterile water and 0.9% normal saline bottles due to leaking at the peel-foil and bottle opening interface. The defect affects 159 units distributed nationwide and internationally.
Product
Medline procedure kits, labeled as: HAND, REF DYNJ902002J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0396-2025·2025-05-07
Levothyroxine Sodium Tablets 88 mcg Recall for Subpotency
Accord Healthcare is recalling Levothyroxine Sodium Tablets 88 mcg (Lot D2300044, expiring 12/2025) nationwide because the tablets are subpotent—below the required strength. Patients on this medication should contact their pharmacy or prescriber.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V293000·2025-05-07
2025 Polestar 3 vehicles recalled for faulty rearview camera display
Polestar is recalling certain 2025 Polestar 3 vehicles because the rearview camera image may not display when the vehicle is in reverse, reducing driver visibility and increasing crash risk.
Product
POLESTAR — POLESTAR POLESTAR 3
Category
Vehicle
Distribution
Distributed nationwide