Bard recalls EnCor Breast Biopsy Probes with leaks and suction problems. Affected units have specific lot numbers. Stop using if you have these probes.
There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
Bard is recalling EnCor Breast Biopsy Probes due to leaks and suction issues that can cause failed sample collection. This affects patients undergoing breast biopsies who use the product as directed.
The probes can leak or have suction problems, which may lead to failed sample collection during breast biopsies. This could result in the need for additional procedures or delays in diagnosis.
Patients who have received a prescription for EnCor Breast Biopsy Probes with specific lot numbers are most at risk. Healthcare providers using these probes for breast biopsies may also be affected.
Check the lot numbers on the packaging: VTCT0306, VTCT0307, VTCU0358 through VTCZ0647, VTDN0035, and VTDN0036. These probes are sold in sterile pouches, 5 per carton, with a prescription.
Look for lot numbers VTCT0306, VTCT0307, VTCU0358 through VTCZ0647, VTDN0035, and VTDN0036 on the packaging.
Bard recalls EnCor Breast Biopsy Probes due to increased complaints about leaks and suction issues that can cause failed sample collection.
Check the lot numbers on the packaging. If you have the affected lot numbers, stop using the probes and contact Bard for instructions.
The probes can leak or have suction problems, which may lead to failed sample collection during breast biopsies, requiring additional procedures or delays in diagnosis.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2209-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2209-2019 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.
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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.
