Bard recalls specific models of biopsy probes due to increased failures like leaks and suction issues. Affected units include lot numbers VTCT0268-0271 and VTCU0340-0341.
Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.
Bard is recalling certain biopsy probes that may fail during medical procedures, causing leaks, suction problems, or failure to collect samples. This recall affects specific lot numbers and is important for medical users to avoid potential complications.
The probes can leak, have suction issues, or fail to obtain samples during medical procedures. This could lead to complications for patients or healthcare providers if the device malfunctions.
Medical professionals using the Bard Biopsy EnCor Probe 7G for procedures are most at risk. Patients using these probes during surgery may experience complications if the device fails.
Check for lot numbers VTCT0268 through VTCT0271 and VTCU0340 through VTCU0341 on the sterile pouches. The product is a single-use probe packaged in sterile pouches.
Look for lot numbers VTCT0268 to VTCT0271 and VTCU0340 to VTCU0341 on the sterile pouches.
The recall is due to increased failures like leaks, suction issues, and failure to obtain samples in medical procedures.
Lot numbers VTCT0268, VTCT0269, VTCT0270, VTCT0271, VTCU0340, and VTCU0341 are affected.
The recall record does not specify a remedy, so no action is required beyond checking the lot numbers.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1431-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1431-2020 from Bard. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.