Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb… — Class II medical device recall Z-2639-2026
Ongoing recall by TELEFLEX LLC, reported 2026-07-08, distributed nationwide. Due to out-of-specification, or potential out-of-specification, levels of endotoxins
| Recall number | Z-2639-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX LLC, Morrisville, NC, United States |
| Recall initiated | 2026-05-07 |
| Classified | 2026-07-01 |
| Reported by FDA | 2026-07-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | PA |
| Quantity | 1,488,700 |
| Reason classes | sterility |
| Lot numbers | 21E1397, 21E1398, 21E1399, 21E1400, 21E1485, 21E1503, 21E1504, 21E1505, 21E1506, 21E1507, 21E1508, 21E1509, 21E1546, 21E1547, 21E1548, 21F1809, 21G2034, 21G2179, 21H2304, 21H2305, 21H2329, 21H2330, 21H2331, 21H2339, 21H2594, 21H2595, 21H2596, 21H2597, 21H2598, 21H2599, 21H2600, 21H2601, 21H2602, 21H2603, 21H2604, 21H2605, 21H2606, 21H2607, 21K3161, 21K3162 and 129 more |
| Model numbers | 200100, 200101, 200102, 200103, 200104, 200105, 200106, 200108, 200110, 200112, 200120, 200121, 200123, 200131 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2639-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.