Drugs & medicalClass II

TAS Medical Inc recalls TISSUE APPROXIMATION SYSTEM (TAS), Models T-4000, T-5000, T-LAP

Tissue approximation straps (zip-ties) have broken before or during implantation so firm developed an interim zip-tie conditioning method submerging zip-ties in 104-degrees F sterile saline solution for 60 min prior to…

Read the official notice →
Date
2025-03-12
Country
United States
Brand
TAS Medical Inc
Product
TISSUE APPROXIMATION SYSTEM (TAS), Models T-4000, T-5000, T-LAP
Classification
Class II
Units
US Nationwide distribution in the states of LA, OK, TN.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

Other drugs & medical recalls in the United States

  1. 2025-03-19
  2. US
    Drugs & medicalClass II

    Nephron Sterile Compounding Center LLC recalls Sodium Chloride Injection 9%, USP, 500 mL, Single-Dose IV Bottle, Rx Only, nephron, 503B outsourcing facility, West…

    Lack of Assurance of Sterility: There is a potential for leakage at the IV bottle port.

    FDA · DrugNephron Sterile Compounding Center LLCUS Nationwide.Official notice →
  3. 2025-03-12
  4. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BD BBL TB Stain Kit K, Catalog (REF): 212522

    One component of the kit was shipped with an expiration date of 30Sep2024 while the Certificate of Analysis (COA) indicated an expiration date of 30Apr2025.

    FDA · DeviceBecton Dickinson & Co.Domestic: AZ, CA, CO, GA, KY, IL, IN, NC, NJ, NY, MA, MD, TX, WA.…Official notice →
  5. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. recalls AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. Manufacturer's Product Numbers…

    Possibility for the obturator to break (separate).

    FDA · DeviceIntegra LifeSciences Corp.US Nationwide distribution in the states of MO, FL, TX, NY, IL, OH, NJ, CA,…Official notice →
  6. US
    Drugs & medicalClass II

    Alcon Research LLC recalls Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05,…

    Customer-designed sterile surgical procedure packs contain latex components as specified; but, the content label sealed within the transparent sterile pouch contains the symbol for a latex-free product. If users or…

    FDA · DeviceAlcon Research LLCUS Nationwide distribution in the states of AK, AR, AZ, FL, MD, MN, NC, NE,…Official notice →
  7. US
    Drugs & medicalClass II

    Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050

    Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.

    FDA · DeviceMurata Vios, Inc.US Nationwide distribution in the states of Florida, Louisiana, Maryland,…Official notice →
  8. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal REF 71-C5100NS Tubing, Suction, Connector; DeRoyal REF 71-C6100NS Tubing, Suction, Connector; DeRoyal REF 71-C7100NS Tubing,…

    Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a…

    FDA · DeviceDeRoyal Industries IncU.S.: IL, MN, NC, PA, and VA O.U.S.: N/AOfficial notice →
See all drugs & medical recalls →