Recall of 1,481,700 US units of Pilling Wecksorb Neurosponges (cotton) due to potential endotoxin levels. Affected models include 200100-200131 with specific UDI codes and batch numbers. No remedy stated in official notice.
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
TELEFLEX LLC is recalling certain Pilling Wecksorb Neurosponges (cotton) because they may contain unsafe levels of endotoxins. These sponges are used in brain and spinal surgery to protect tissue. The recall affects specific model numbers and batch codes listed in the notice.
The recall is due to potential out-of-specification levels of endotoxins in the cotton sponges. Endotoxins are bacterial components that can cause infections or adverse reactions when introduced into the body, especially during surgical procedures.
Surgical teams and hospitals that use Pilling Wecksorb Neurosponges (cotton) for brain or spinal procedures are likely affected. Patients receiving these sponges during surgery may be at risk if the recalled items were used.
Check for model numbers 200100-200131 with specific UDI codes and batch numbers listed in the recall notice. The sponges are used in brain and spinal surgery to protect tissue.
Review the model numbers and batch codes listed in the recall notice to determine if your item is affected.
The recall is due to potential out-of-specification levels of endotoxins in the cotton sponges, which could cause infections or adverse reactions during surgery.
Affected models include 200100-200131 with specific UDI codes and batch numbers listed in the recall notice.
The official recall notice does not specify a remedy, so no action is required beyond checking if your product is affected.
We’ve drafted a message you can send Pilling Wecksorb to request your refund or repair — edit it as you like.
Subject: Recall Z-2639-2026 — Pilling Wecksorb Pilling Wecksorb Hello, I own a Pilling Wecksorb that is covered by recall Z-2639-2026 from Pilling Wecksorb. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
