Teleflex recalls

9 official recalls and safety alerts involving Teleflex since 2022-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Teleflex or the relevant agency.

1. 2026-07-08
2. US
   Drugs & medicalClass II

   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
4. US
   Drugs & medicalClass II

   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
6. US
   Drugs & medicalClass I

   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. 2023-06-07
8. US
   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…

   FDA · DeviceTELEFLEX LLCworldwideOfficial notice →
9. 2023-05-24
10. US
    Drugs & medicalClass II

    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 →
11. 2023-02-01
12. 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 →
13. 2023-01-04
14. US
    Drugs & medicalClass II

    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 →
15. 2022-11-23
16. US
    Drugs & medicalClass II

    TELEFLEX LLC recalls Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.

    Product may not be sterile

    FDA · DeviceTELEFLEX LLCTN, CA, NC, TX, FL, OH, MO, IL, OROfficial notice →
17. 2022-10-26
18. US
    Drugs & medicalClass I

    TELEFLEX LLC recalls Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use

    Incidents of device splitting or detaching during use

    FDA · DeviceTELEFLEX LLCUS nationwide distributionOfficial notice →