Drugs & medicalClass II

TELEFLEX LLC recalls Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or…

Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applier. With this step…

Read the official notice →
Date
2023-06-07
Country
United States
Brand
Teleflex
Product
Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or…
Classification
Class II
Units
worldwide
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 Details may be shortened or out of date; the official notice is the authoritative source.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 recalls

  1. 2026-07-08
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    TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton)…

    Due to out-of-specification, or potential out-of-specification, levels of endotoxins

    FDA · DeviceTELEFLEX LLCWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  3. 2023-07-12
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    TELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor

    There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).

    FDA · DeviceTELEFLEX LLCNationwide and Australia, Canada, S. Korea, SingaporeOfficial notice →
  5. 2023-07-05
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    TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085

    Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

    FDA · DeviceTELEFLEX LLCUS Nationwide distribution including Puerto Rico.Official notice →
  7. 2023-05-24
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    TELEFLEX LLC recalls Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tracts of femoral…

    The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.

    FDA · DeviceTELEFLEX LLCUS NationwideOfficial notice →
  9. 2023-02-01
  10. US
    Drugs & medicalClass II

    TELEFLEX LLC recalls Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal; b. Endotracheal Tube…

    Potential for pilot balloon non-inflation or cuff non-deflation.

    FDA · DeviceTELEFLEX LLCWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →
  11. 2023-01-04
  12. US
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    TELEFLEX LLC recalls Pilling Wecksorb Cylindrical Sponges

    Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.

    FDA · DeviceTELEFLEX LLCDomestic distribution to IL, MS, PA, TN.Official notice →
All 9 Teleflex recalls →

Other drugs & medical recalls in the United States

  1. 2023-06-07
  2. US
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    NRT X-RAY A/S recalls Intelli-C, Left side suspended Tabletop, REF: 03400010

    There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.

    FDA · DeviceNRT X-RAY A/SUS Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA,…Official notice →
  3. US
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    Elekta, Inc. recalls Elekta Medical Linear Accelerator (ELMA) included in the below platforms: a. Elekta Infinity; b. Versa HD; c. Elekta Synergy

    A component within a limited number of Elekta Linacs has been realized to be non-compliant to IEC 60601

    FDA · DeviceElekta, Inc.Worldwide distribution. US distribution to AR, IN, LA, OK, TN, VA, WA.…Official notice →
  4. US
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    Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN) 50 with affected Assay Data Disk (ADD) for Data…

    Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation (GEN) 50, results in delay of testing

    FDA · DeviceOrtho-Clinical Diagnostics, Inc.Nationwide Foreign: Brazil, Chile, ColombiaOfficial notice →
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    Maquet Medical Systems USA recalls QUADROX -i Neonatal, Oxygenator used during cardiopulmonary bypass Model Item No. HMO 10000-USA 701070412 HMO 11000-USA 701070416

    Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis,…

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    Cytrellis Biosystems, Inc. recalls Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended for the treatment of moderate and…

    Irregular core patterns could cause potential overlap of cores at the 8% setting, potentially leading to prolonged healing, irregularities in patient skin texture post-treatment, and/or scarring.

    FDA · DeviceCytrellis Biosystems, Inc.NationwideOfficial notice →
See all drugs & medical recalls →