Wilson-Cook Medical recalls Captura Serrated Biopsy Forceps with Spike (DBF-2.4SN-230SP-20-S) due to mislabeling with no-spike models. This could lead to incorrect use in medical procedures.
The product is being recalled because Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S) were mislabeled as Captura Serrated Large Forcep-No Spike (DBF-2.4SL-230-20-S) and Captura Serrated Large Forcep-No Spike (DBF-2.4SL-230-20-S) were mislabeled as Captura Serrated Forceps with Spike (DBF-2.4SN-230SP-20-S).
Wilson-Cook Medical is recalling a specific type of biopsy forceps because they were mislabeled. This could cause doctors to use the wrong type of forceps during medical procedures, potentially leading to complications.
The forceps were mislabeled as either the spiked or no-spike version. Using the wrong type could lead to improper tissue handling during biopsies, potentially causing injury or complications.
Medical professionals who use these forceps for biopsies may be affected. Patients undergoing procedures with these forceps could be at risk if mislabeled models are used.
Check for the model number DBF-2.4SN-230SP-20-S on the product. The lot number W4035256 is also associated with this recall.
Look for the model number DBF-2.4SN-230SP-20-S and lot number W4035256 on the forceps.
The forceps were mislabeled as either the spiked or no-spike version, which could lead to incorrect use during medical procedures.
Check the product label for the model number DBF-2.4SN-230SP-20-S and lot number W4035256. If you have the correct model, no action is needed.
Using the wrong type of forceps could lead to improper tissue handling, but the recall is for mislabeling, not an immediate hazard.
We’ve drafted a message you can send Wilson-Cook Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0774-2019 — Wilson-Cook Medical Wilson-Cook Medical Hello, I own a Wilson-Cook Medical that is covered by recall Z-0774-2019 from Wilson-Cook Medical. 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.
