Drugs & medicalClass I

TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The…

The firm received reports indicating PTD tip separation during use.

Read the official notice →
Date
2022-02-23
Country
United States
Brand
Teleflex Medical
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The…
Classification
Class I
Units
Worldwide distribution: US Nationwide and the countries of AU, BE, CA, CL, CZ,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Teleflex Medical recalls

  1. 2022-06-01
  2. US
    Drugs & medicalClass II

    TELEFLEX MEDICAL INC recalls (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck…

    Reports received of torn corrugated breathing tubes.

    FDA · DeviceTELEFLEX MEDICAL INCWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
All 2 Teleflex Medical recalls →

Other drugs & medical recalls in the United States

  1. 2022-02-23
  2. US
    Drugs & medicalClass III

    Microbiologics Inc recalls KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)

    Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating…

    FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide and the countries of Canada, South…Official notice →
  3. US
    Drugs & medicalClass II

    Hill-Rom, Inc. recalls Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015

    Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

    FDA · DeviceHill-Rom, Inc.Worldwide distribution - US Nationwide and the countries of Austria, Austria,…Official notice →
  4. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Olympus flexible…

    The detergent and alcohol tank tubing may have been incorrectly assembled in the OER-Elite. If the tubing is incorrectly assembled, alcohol will be dispensed instead of detergent for the cleaning cycle and detergent…

    FDA · DeviceOlympus Corporation of the AmericasNationwideOfficial notice →
  5. US
    Drugs & medicalClass I

    Vyaire Medical recalls bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista 1000/1000e ventilator is…

    Potential cessation in ventilation can occur under specific conditions.

    FDA · DeviceVyaire MedicalWorldwide distribution - US Nationwide distribution in the states of AL, CA,…Official notice →
  6. US
    Drugs & medicalClass I

    BASE 10 GENETICS INC recalls RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of RNAstill MTM specimen…

    The product does not have 510(k) clearance.

    FDA · DeviceBASE 10 GENETICS INCUS Nationwide distribution in the states of AL, CO, FL, GA, ID, IN, KY, MD,…Official notice →
  7. US
    Drugs & medicalClass II

    Teligent Pharma, Inc. recalls Erythromycin Topical Gel USP, 2%, Net Wt 30 g tube, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, Distributed by:…

    Failed Impurities/Degradation Specifications: Lot not meeting specification for Unknown Max Related Compounds.

    FDA · DrugTeligent Pharma, Inc.Nationwide in the USA.Official notice →
See all drugs & medical recalls →