The Recall Desk

State

Texas product recalls

73,478 recalls have nationwide distribution and so reach Texas. 12,437 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,437
Critical
1,720
Severe
2,926
Most recent
2026-10-14

Of the 12,437 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 12,437 recalls whose distribution notice names Texas specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23551–23575 of 85915

  • HighFDA (Drugs)·D-0949-2022·2022-06-01

    FDA Recalls Amino Blend Injectable Vials Due to Sterility Concerns

    Olympia Compounding Pharmacy is recalling Amino Blend injectable vials due to lack of assurance of sterility. Approximately 7,761 vials were distributed nationwide. The FDA has classified this as a Class II recall.

    Product
    Amino Blend Glutamine 30 mg/mL Ornithine HCL 50 mg/mL Arginine HCL 100 mg/mL Lysine HCL 50 mg/mL Citrulline 50 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835.NDC 73198-0129-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0901-2022·2022-06-01

    Olympia Compounding Pharmacy Recalls Papaverine-Phentolamine Injectable Due to Sterility Concerns

    Olympia Compounding Pharmacy is recalling SB-6, a compounded injectable medication, due to lack of assurance of sterility. The recall affects 874 vials distributed nationwide, in Puerto Rico, and the US Virgin Islands.

    Product
    SB-6 Papaverine 30 mg/mL Phentolamine 3 mg/mL PGE 60 mcg/mL, Packaged in a) 5 mL Multi-Dose vial, NDC 73198-0025-05; b) 10 mL, Multi-Dose vial, NDC 73198-0025-10; Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0924-2022·2022-06-01

    Dexpanthenol 250 mg/mL Injectable Solution Recalled for Sterility Failure

    Olympia Compounding Pharmacy is recalling 1,296 vials of Dexpanthenol 250 mg/mL injectable solution distributed nationwide due to lack of assurance of sterility in the manufacturing process.

    Product
    Dexpanthenol 250 mg/mL Multi-Dose 30 mL Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0070-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0912-2022·2022-06-01

    FDA Recalls Testosterone Cypionate Injection Vials for Lack of Sterility Assurance

    Olympia Compounding Pharmacy recalled Testosterone Cypionate injection vials due to lack of sterility assurance. The affected lot was distributed nationwide. Patients should contact their healthcare provider immediately.

    Product
    Testosterone Cypionate 200 mg/mL in Sesame Oil, Packaged in a) 5 mL Multi-Dose vial NDC, 73198-0055-05; b) 10 mL Multi-Dose vial NDC 73198-0055-10; Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0926-2022·2022-06-01

    Injectable Folic Acid and Hydroxocobalamin Recalled Due to Sterility Concerns

    Olympia Compounding Pharmacy is recalling 2,441 vials of Folic Acid 1 mg/mL Hydroxocobalamin 1 mg/mL injectable due to lack of sterility assurance. The affected vials were distributed nationwide, in Puerto Rico, and the US Virgin Islands.

    Product
    Folic Acid 1 mg/mL Hydroxocobalamin 1 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0112-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0940-2022·2022-06-01

    Injectable pharmaceutical vial recalled due to sterility assurance failure

    Olympia Compounding Pharmacy is recalling an injectable medication vial due to lack of sterility assurance. The recall affects 606 vials distributed nationwide, Puerto Rico, and US Virgin Islands.

    Product
    NB-343 Papaverine 30 mg/mL Phentolamine 3 mg/mL PGE 30 mcg/mL, Multi-Dose 10 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0010-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V391000·2022-06-01

    Elgin RegenX Vehicles Recalled for Loose Fan Assembly Bolts

    Elgin Sweeper is recalling 2018-2022 RegenX vehicles because improperly tightened fan assembly bolts may detach, creating a road hazard and increasing crash risk.

    Product
    ELGIN — ELGIN REGENX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0915-2022·2022-06-01

    Vitamin D3 Injectable Recalled Due to Sterility Assurance Issues

    Olympia Compounding Pharmacy is recalling Vitamin D3 injectable vials due to lack of sterility assurance. A total of 3,083 vials were distributed nationwide.

    Product
    Vitamin D3 (50,000 IU/mL)Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0075-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0946-2022·2022-06-01

    Pyridoxine Injection Vials Recalled Due to Sterility Concerns

    Olympia Compounding Pharmacy is recalling 1,306 vials of Pyridoxine HCL 100 mg/mL injection due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and US Virgin Islands.

    Product
    Pyridoxine HCL 100 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0066-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0936-2022·2022-06-01

    Methylcobalamin Injectable Recalled for Lack of Sterility Assurance

    Olympia Compounding Pharmacy recalls Methylcobalamin 5 mg/mL injectable due to lack of assurance of sterility. Approximately 12,800 vials were distributed nationwide.

    Product
    Methylcobalamin 5 mg/mL, Packaged as a) Multi-Dose 10mL vial, NDC 73198-0051-10; b) Multi-Dose 30mL vial, NDC 73198-0051-30, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1121-2022·2022-06-01

    Unclearred VerifyNow P2Y12 Platelet Test Variant Distributed to Healthcare Providers

    Accriva Diagnostics distributed an unclearred variant of the VerifyNow P2Y12 platelet test that displays different results than the FDA-cleared device. A correction formula has been provided to healthcare providers.

    Product
    The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 receptor blockade. Substances known to specifically block the P2Y12 receptor include ticagrelor and the thienopyridine class of drugs, including clopidogrel and prasugrel.1-8 The test is based upon the ability of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1124-2022·2022-06-01

    HydroMARK Breast Biopsy Marker Label Mismatch on Patient Documentation

    Devicor Medical Products is recalling 90 HydroMARK Breast Biopsy Markers due to mismatched patient labels that incorrectly identify the product model. The small patient label identifies the device as model 4010-05-08-T3, while the correct model is 4010-05-08-T4.

    Product
    HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2022·2022-06-01

    Gibeck Humid-Vent Breathing Filters Recalled for Torn Corrugated Tubes

    Teleflex Medical is recalling Gibeck brand respiratory filters due to reports of torn corrugated breathing tubes. No injuries have been reported.

    Product
    (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19061, sterile; (4) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0903-2022·2022-06-01

    Pharmaceutical Diluent Recalled for Lack of Sterility Assurance

    Olympia Compounding Pharmacy is recalling pharmaceutical diluent vials due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and US Virgin Islands.

    Product
    Diluent for Reconstitution Multi-Dose 10 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0113-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0938-2022·2022-06-01

    Myers Cocktail Injectable Vials Recalled for Sterility Assurance Issues

    Olympia Compounding Pharmacy is recalling Myers Cocktail injectable vials due to lack of assurance of sterility. The recall affects approximately 13,679 vials distributed nationwide.

    Product
    Myers Cocktail, Magnesium Chloride 9.65 mg/mL Dexpanthenol 4.07 mg/mL Thiamine HCL 1.62 mg/mL Riboflavin-5-Phosphate 3.23 mg/mL Pyridoxine HCL 1.63 mg/mL Niacinamide 1.62 mg/mL Calcium Gluconate 4.07 mg/mL Ascorbic Acid 64.4 mg/mL, Single-Dose 10 mL vial, Rx Only, Olympia…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1119-2022·2022-06-01

    Steris Non-Woven Sponges recalled; product not approved for US distribution

    Steris Corporation is recalling 152 cases of Ultra Pure Non-Woven Sponges because the product was not approved for release for US distribution.

    Product
    Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2,000 per case 10 sleeves of 200 4 in x 4 in / 10.2 cm x 10.2 cm Model Number: ENC4100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1118-2022·2022-06-01

    Steris Recalls Ultra Pure Non-Woven Sponges for Unapproved Distribution

    Steris Corporation is recalling 103 cases of Ultra Pure Non-Woven Sponges (Lot 202108) distributed nationwide because the product was released without FDA approval. Customers should discontinue use and contact the manufacturer.

    Product
    Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5,000 per case 25 sleeves of 200 2 in x 2 in / 5.1 cm x 5.1 cm Model Number: ENC100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0896-2022·2022-06-01

    Drug Recall: Tivicay Tablets with Incorrect Expiration Date on Label

    GlaxoSmithKline is recalling 328 bottles of Tivicay (dolutegravir) tablets nationwide due to incorrect expiration date labeling. The label shows January 2027 but the correct expiration date is September 2026.

    Product
    TIVICAY — TIVICAY (DOLUTEGRAVIR SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0888-2022·2022-06-01

    Zonisamide Capsules USP recalled for quality control system deviation

    Direct Rx is recalling Zonisamide Capsules USP 100 mg, lot 23JY2124, nationwide due to gaps in the quality control microbiology laboratory that could affect product verification.

    Product
    Zonisamide Capsules USP, 100 mg, 90-count bottle, Rx Only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, NDC 61919-775-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1125-2022·2022-06-01

    Medical device labeling error: KWIK-STIK® plus Clostridium perfringens

    Microbiologics Inc recalled 8 units of KWIK-STIK® plus Clostridium perfringens due to a labeling error. The affected lot (801-44-4) was distributed to laboratories in the United States and internationally.

    Product
    KWIK-STIK" plus: Clostridium perfringens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V389000·2022-05-31

    TM Industries Recalls 2021-2022 TrailManor 2518 Series Travel Trailers

    TM Industries is recalling 2021-2022 TrailManor 2518 series travel trailers because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    TRAILMANOR — TRAILMANOR 2518 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V388000·2022-05-30

    Escape Trailer Recalls 2018-2021 Models Due to Gas Leak Risk

    Escape Trailer is recalling 2018-2021 travel trailers because aluminum burner tubes can fracture, causing a gas leak that may lead to fire.

    Product
    ESCAPE — ESCAPE, ESCAPE RV ESCAPE 5.0, ESCAPE 19, ESCAPE 17, ESCAPE 21
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V387000·2022-05-30

    2021-2022 Escape Travel Trailers Recalled for Cracked LP Gas Fittings

    Escape Trailer is recalling 2021-2022 Escape travel trailers (models 17, 19, 21, and 5.0TA) due to cracked quick disconnect fittings in the LP gas system that may cause a gas leak and fire hazard.

    Product
    ESCAPE — ESCAPE ESCAPE 19, ESCAPE 5.0, ESCAPE 17, ESCAPE 21
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E047000·2022-05-28

    R.H. Sheppard Recalls Steering Gears Due to Fracture Risk

    R.H. Sheppard is recalling specific steering gears that may have been assembled incorrectly, posing a risk of fracture and loss of steering control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide