The Recall Desk

State

Texas product recalls

73,388 recalls have nationwide distribution and so reach Texas. 12,434 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,434
Critical
1,720
Severe
2,926
Most recent
2026-10-07

Of the 12,434 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 2,926 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,434 recalls whose distribution notice names Texas specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22101–22125 of 85822

  • SevereFDA (Devices)·Z-1399-2022·2022-08-17

    FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance

    The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1400-2022·2022-08-17

    Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance

    Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E069000·2022-08-17

    S&B Diesel Fuel Tank Recall for Insufficient Driveline Clearance

    S&B Filters is recalling certain diesel fuel tanks for RAM Mega Cab vehicles due to insufficient clearance that may cause fuel leaks and fire risk.

    Product
    FUEL SYSTEM, DIESEL:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1311-2022·2022-08-17

    Triple Antibiotic Ointment Recalled Due to Improper Storage

    McKesson Medical-Surgical Inc. is recalling Triple Antibiotic Ointment due to storage deviations that violated drug label specifications and current good manufacturing practices.

    Product
    Triple Antibiotic Ointment, Bacitracin zinc, Neomycin sulfate, Polymixin B sulfate, First Aid Antibiotic, Triple Antibiotic Ointment, 144 packets per box, Net wt. per packet 0.5 g, Honeywell Safety Products, NDC 0498-0750-36.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1539-2022·2022-08-17

    Natierra Organic Freeze-Dried Blueberries Recalled for Lead Contamination

    Natierra Nature & Earth Organic Blueberries are recalled due to elevated lead levels detected by Maryland Department of Health testing. The recall affects 22,014 units distributed nationwide.

    Product
    Natierra Nature & Earth Organic Blueberries Ingredients: Organic Freeze-Dried Blueberries NET WT 12 oz (34g) Distributed by Natierra Van Nuys, CA 91405-1545 Certified Organics by SCS Global Services Product of US, Canada, Poland, Estonia, Romania
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1328-2022·2022-08-17

    Difluprednate eye drops recalled for defective container closure affecting sterility

    Cipla is recalling Difluprednate ophthalmic emulsion nationwide due to defective container closures that compromise sterility assurance. Patients using the affected lot should discontinue use and contact their healthcare provider.

    Product
    DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V630000·2022-08-17

    PACCAR Recalls 2021 Peterbilt 220 and 2022 Kenworth K270 Trucks

    PACCAR is recalling 2021 Peterbilt 220 and 2022 Kenworth K270 trucks because software may prevent stability control commands from processing during regenerative braking, increasing crash risk.

    Product
    PETERBILT — PETERBILT, KENWORTH 220, K270
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2022·2022-08-17

    HAIOU Retractable Safety Syringes Recalled for Needle Detachment Risk

    HAIOU retractable safety syringes are recalled due to reports of needle detachment from the syringe after injection and failure to retract, increasing needle stick injury risk. Approximately 4.05 million units are affected.

    Product
    HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-25G25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1330-2022·2022-08-17

    Prednisone Tablets Recalled for Contamination With Wrong-Strength Tablets

    Strides Pharma is recalling Prednisone 20 mg tablets due to contamination with 2.5 mg tablets. No illnesses have been reported, but patients may receive incorrect doses.

    Product
    PREDNISONE — PREDNISONE (PREDNISONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1315-2022·2022-08-17

    Eye-stream Eye Wash Solution Recalled for Improper Storage

    Mckesson Medical-Surgical has recalled Eye-stream eye wash solution nationwide due to storage conditions outside drug label specifications.

    Product
    Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1515-2022·2022-08-17

    Roche cobas e801 Analyzer Recall: Software Defect Affects Test Results

    Roche is recalling approximately 965 cobas e801 Immunoassay Analyzers nationwide due to a software issue that impacts Pre-Wash test signals and results for six diagnostic assays. No injuries or illnesses have been reported.

    Product
    cobas e801 Immunoassay Analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1331-2022·2022-08-17

    FentaNYL Citrate IV solution recalled due to sterility assurance concerns

    SterRx is recalling FentaNYL Citrate intravenous bags (10 mcg/mL) due to lack of assurance of sterility. The recalled lot (CHI, expiring December 2022) was distributed nationwide.

    Product
    FentaNYL Citrate in 0.9% Sodium Chloride 1 mg per 100 mL (10 mcg per mL) IV bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY, 12903, NDC 70324-327-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1511-2022·2022-08-17

    GE Healthcare CT, PET, and NM Patient Tables May Drop During Service

    GE Healthcare patient tables used in CT, PET, and NM systems can drop during service if technicians remove incorrect screws without appropriate supports, potentially injuring service personnel.

    Product
    Service manuals for the CT, PET, or NM table as follows: GT1700/GT1700V/VT1700, GT2000/VT2000, GT2000x/VT2000x, High Capacity Table, Lite Table, Kunlun Table, Global PET-CT Table, NP Table, P2005AA Table, LCT Table, CTE TWIN TABLE Assy. All devices are patient tables for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V629000·2022-08-17

    2022 Genuine Scooter Handlebar Vibration May Cause Loss of Control

    Genuine Scooters is recalling certain 2022 NIU MQiGT EVO scooters due to excessive handlebar vibration. The vibration may cause rider fatigue or loss of vehicle control, increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER NIU MQIGT EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1317-2022·2022-08-17

    FDA Recalls ZADITOR Eye Drops Due to Improper Storage Conditions

    ZADITOR eye drops were stored outside FDA label specifications in a nationwide Class II recall affecting 9 boxes distributed by McKesson Medical-Surgical Inc.

    Product
    ZADITOR — ZADITOR (KETOTIFEN FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1541-2022·2022-08-17

    Whey Protein Powder Recalled for Undeclared Milk Allergen

    Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Vanilla Bean due to missing milk allergen declaration on the label. Consumers with milk allergies may be at risk.

    Product
    Aivia Whey Protein+ Power Herbs Vanilla Bean, NET WT. 1.33 LBS (602 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22712 5 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1307-2022·2022-08-17

    Lorazepam injection vials recalled nationwide for manufacturing specification failures

    Hikma Pharmaceuticals is recalling approximately 4.7 million vials of Lorazepam injection nationwide after finding out-of-specification related compounds during quality testing. The affected lots expire between June and August 2023.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1332-2022·2022-08-17

    Fentanyl Citrate IV Bags Recalled Due to Sterility Assurance Failure

    SterRx is recalling 360 bags of fentanyl citrate IV medication due to lack of assurance of sterility. No illnesses have been reported.

    Product
    fentaNYL Citrate in 0.9% Sodium Chloride, 2.5 mg per 250 mL, (10 mcg per mL) IV bags, Rx Only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-327-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1540-2022·2022-08-17

    Aivia Whey Protein Chocolate Recalled for Undeclared Milk Allergen

    Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Chocolate because the label declares whey but fails to declare milk. Approximately 2,747 bags were distributed nationwide.

    Product
    Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22711 8 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2022·2022-08-17

    MetaFix hip stem mislabeled with wrong size and batch information

    A Corin MetaFix hip stem (size 7 collarless) was incorrectly labeled as a size 3 collared stem with wrong batch information. The labeling error creates risk during surgical implantation.

    Product
    Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1310-2022·2022-08-17

    Lorazepam Injection Recalled for Out-of-Specification Impurities and Degradation

    Hikma Pharmaceuticals is recalling 82,700 vials of Lorazepam Injection due to failed quality specifications for impurities and degradation. Lot #070096 (expired July 2023) was distributed nationwide.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1326-2022·2022-08-17

    FDA Recalls Sterile Alcohol Prep Pads Due to Improper Storage

    Mckesson Medical-Surgical is recalling ALCOHOL PREP sterile alcohol prep pads nationwide because they were stored outside manufacturer specifications, potentially compromising sterility. FDA classified this as a Class II recall.

    Product
    ALCOHOL PREP — ALCOHOL PREP (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V631000·2022-08-17

    2023 Kenworth and Peterbilt trucks recalled for engine control failure

    PACCAR Incorporated is recalling certain 2023 Kenworth and Peterbilt commercial trucks because the engine control module may short-circuit, causing the engine to stall unexpectedly. An engine stall while driving increases the risk of a crash.

    Product
    PETERBILT — PETERBILT, KENWORTH 520, 579, T680, T800B
    Category
    Vehicle
    Distribution
    Distributed nationwide