# FDA recall Z-2639-2026

> **TELEFLEX LLC** · Class II · device recall initiated 2026-05-07.

## Product

Brand Name: Pilling Wecksorb  Product Name: Pilling Wecksorb Neurosponges (Cotton)  Pilling¿ Wecksorb Neurosponge Strips (Cotton)  Model/Catalog Number:  200100  200101  200102  200103  200104  200105  200106  200108  200110  200112  200120  200121  200123  200131      Software Version: N/A  Product Description: Wecksorb Neurosponges are made of an absorbent cotton material. Certain Neurosponge varieties are available with an x-ray detectable thread to assist with location within the surgical site. Some Neurosponges (patties) have a string for accountability during the post-surgical verification process. Wecksorb Neurosponges are for use in the protection of tissue during surgical procedures; tissues include the brain and other central nervous system tissues.    Neuro sponges are used during cranial and spine surgery to moisten the dura or to cushion against bone edges.  They are also used to protect brain tissue under the dura or elsewhere during incision.    Component: N/A

## Reason for recall

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

## Distribution

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WV. The country of Panama.

## Key facts

- **Recall number:** Z-2639-2026
- **Recalling firm:** TELEFLEX LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-07
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2639-2026

## Citation

> MORVS. FDA recall Z-2639-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2639-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*