State

Texas product recalls

73,092 recalls have nationwide distribution and so reach Texas. 12,427 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,427
Critical: 1,720
Severe: 2,421
Most recent: 2026-09-23

Of the 12,427 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 2,421 (19%) are Severe.

Which agencies issued them

These figures cover only the 12,427 recalls whose distribution notice names Texas specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9726–9750 of 85519

HighFDA (Devices)·Z-0487-2025·2024-11-27
Ethicon Recalls Monocryl Sutures Due to Component Mix-Up
Ethicon, Inc. is recalling 16,524 units of Monocryl sutures because a manufacturing error may result in incorrect needle types, sizes, or suture lengths.
Product
MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular and neurological tissues, microsurgery or ophthalmic surgery.
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0501-2025·2024-11-27
OrganOx metra Liver Perfusion System Recalled for Battery Damage
OrganOx Ltd is recalling 20 metra liver perfusion systems because battery movement caused a cell to short against the retention bracket.
Product
OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers. Model/Catalog Number: D0003 The OrganOx metra is a transportable device intended to be used to sustain donor livers destined for transplantation in a functioning state for a total
Category
Medical Device
Distribution
10 states
HighFDA (Devices)·Z-0484-2025·2024-11-27
Maquet Cardiovascular Recalls Acrobat-i Positioners Due to Sterility Concerns
Maquet Cardiovascular is recalling 14,338 Acrobat-i Positioners because manufacturing deviations compromised the sterile barrier, meaning sterility cannot be assured during the product's 2-year shelf life.
Product
Acrobat-i Positioner. Model Number C-XP-5000Z
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V895000·2024-11-27
Forest River Recalls 2025 Motorhomes Due to Taillight Overheating and Failure
Forest River is recalling 2025 Concord, Entourage, Freelander, and Leprechaun motorhomes because taillights may overheat and fail to illuminate, increasing crash risk.
Product
FOREST RIVER — FOREST RIVER FREELANDER, CONCORD, LEPRECHAUN, ENTOURAGE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2025·2024-11-27
Acrobat SUV Vacuum Stabilizer System Sterile Barrier Compromise Recall
Maquet Cardiovascular is recalling the Acrobat SUV Vacuum Stabilizer System (Model C-OM-9000Z) due to manufacturing deviations that compromise the sterile barrier. Sterility cannot be assured during the 2-year shelf life, affecting approximately 10,778 units.
Product
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0140-2025·2024-11-27
Great Value Cheese Danish Recalled for Plastic Pieces
Great Value Cheese Danish is being recalled due to plastic pieces found in the product. Consumers who purchased this item should discard it.
Product
Great Value Cheese Danish 16.5 oz UPC 078742201177, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighNHTSA·24E100000·2024-11-27
Chrysler Recalls Brake Hydraulic Control Units Due to System Failure Risk
Chrysler is recalling specific MOPAR Brake Hydraulic Control Units that may fail, causing loss of anti-lock brakes, stability control, and traction control.
Product
SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0145-2025·2024-11-27
La Bonne Vie Camembert cheese recalled for potential Listeria contamination
La Bonne Vie Camembert 8oz cheese (UPC 820581678616, BBD 12/24/2024) is being recalled due to potential Listeria monocytogenes contamination. Approximately 70 cases were distributed across 12 U.S. states.
Product
La Bonne Vie Camembert 8oz UPC 820581678616; 6 retail units per case
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-0471-2025·2024-11-27
Injection Needles Recalled for Manufacturing Debris Blocking Medication Flow
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris inside the needle shaft that blocks medication flow. The affected lot was distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0496-2025·2024-11-27
Siemens Atellica CH Cuvette Segment manufacturing defect may impact lab test accuracy
Manufacturing defects in Siemens Atellica CH Cuvette Segments may cause inaccurate laboratory test results for seven analytes across 9,729 units.
Product
Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain and incubate the sample reaction volumes and present them to each processing step. Siemens Material Number(SMN): 11099326 All lots starting with N15 or 15 are expected to have the defect.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0055-2025·2024-11-27
Prescription Dextroamphetamine Patches Recalled for Defective Adhesive System
Noven Pharmaceuticals Inc is recalling 685 boxes of XELSTRYM (dextroamphetamine) transdermal patches nationwide due to a defect in the adhesive delivery system. The product does not meet manufacturing specifications.
Product
XELSTRYM — XELSTRYM (DEXTROAMPHETAMINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0060-2025·2024-11-27
Docusate Sodium 250 mg softgels recalled due to defective blister packaging
Safecor Health is recalling Docusate Sodium 250 mg softgels due to manufacturing defects where blister card-foils separated from the medication cavity, potentially compromising product integrity.
Product
Docusate Sodium 250 mg, 1 Softgel in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-101-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2025·2024-11-27
Posi-Stop Injection Needles Recalled Due to Manufacturing Debris Blocking Injection Flow
Hobbs Medical recalls Posi-Stop injection needles because manufacturing debris can block the needle, preventing injection solutions from flowing properly. Affected units were distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0479-2025·2024-11-27
CAIRE FreeStyle Comfort Portable Oxygen Concentrator Battery Charging Failure
CAIRE FreeStyle Comfort portable oxygen concentrators may fail to recharge their batteries, potentially leaving patients without access to supplemental oxygen. Twenty-three units have been recalled.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-101.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2025·2024-11-27
CAIRE FreeStyle Comfort Oxygen Concentrators Recalled for Battery Charging Failure
Caire recalls 739 FreeStyle Comfort portable oxygen concentrators that may fail to recharge their batteries. The devices were distributed in the US, Puerto Rico, Israel, and Peru.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2025·2024-11-27
Philips Vue PACS Diagnostic Viewer Software Recall for Calculation Errors
Philips is recalling Vue PACS Diagnostic Viewer software versions 12.1.5 to 12.2.8.454 because a defect may cause incorrect ischemic map calculations, potentially leading to misdiagnosis.
Product
Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to 12.2.8.454 software Model Number: 1149418 Intended use is to provide completely scalable local and wide area PACS (Picture Archiving and Communication System) solutions for hospital and related institutions/sites.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0049-2025·2024-11-27
Guaifenesin-Dextromethorphan Cough Syrup Recalled for Failed Impurity Specifications
Major Pharmaceuticals is recalling Guaifenesin Dextromethorphan Syrup nationwide for specific lots that failed to meet impurity and degradation specifications. Consumers should contact their pharmacist if they possess affected lots.
Product
Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2025·2024-11-27
Ramipril Capsule Medication Recalled Over Unapproved Vendor Manufacturing Deviations
Lupin Pharmaceuticals is recalling 357,414 bottles of Ramipril 10 mg capsules due to CGMP deviations where the active pharmaceutical ingredient was sourced from an unapproved vendor. The affected product was distributed to 30 wholesalers with potential nationwide distribution.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0050-2025·2024-11-27
Guaifenesin Dextromethorphan Syrup Recalled for Failed Quality Specifications
Major Pharmaceuticals has recalled Guaifenesin Dextromethorphan Syrup due to failed impurity and degradation specifications. Three lot numbers were distributed nationwide.
Product
Guaifenesin Dextromethorphan Syrup, 100 mg/10mg per 5 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7134-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2025·2024-11-27
Posi-Stop Injection Needle Recalled Due to Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Lot H11-23-057) because some units contain manufacturing debris that blocks the needle opening, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0488-2025·2024-11-27
EnChroma Safety Glasses recalled for defective impact protection
EnChroma Inc recalls 53 units of safety glasses with Rx indoor lenses that fail impact safety standards, posing a risk of eye injury. Affected models include Martinez Cx1 Indoor Rx, Summit Indoor Rx, and Martinez Black Cx Rx.
Product
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor Rx, Cx.PC.IN.SUM.BK.Rx; Martinez Black Cx Rx, Cx-3.PC.PT.MTZ.BK.Rx
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2025·2024-11-27
Posi-Stop Injection Needles recalled for manufacturing debris blockage
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris that can block needle flow. Some units may contain debris in the inner sheath that prevents injection solutions from functioning properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0376-2025·2024-11-27
Baxter MiniCap PD Transfer Set Recalled for Potential PCB Exposure
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0380-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0052-2025·2024-11-27
FDA recalls Ramipril 2.5 mg capsules for manufacturing control deviations
Lupin Pharmaceuticals is recalling Ramipril 2.5 mg capsules after sourcing the active ingredient from an unapproved vendor. Approximately 112,770 bottles were distributed to wholesalers nationwide.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide