Becton Dickinson recalls PCEA ASV Yellow Microbore administration sets (catalog numbers 30893, 30893-07) due to potential leaks between the male luer lock and yellow tubing. Affected units may leak during use, requiring replacement.
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
Becton Dickinson is recalling PCEA ASV Yellow Microbore administration sets (catalog numbers 30893 and 30893-07) because they can leak between the male luer lock and yellow tubing. This leak risk could cause contamination or improper medication delivery if the set is used for patient care.
The microbore tubing may leak between the male luer lock connection and the yellow striped tubing. This leak could lead to contamination of the medication or improper delivery if the set is used for patient intravenous therapy.
Healthcare professionals and patients using the PCEA ASV Yellow Microbore administration sets for intravenous therapy. Those who have the specific catalog numbers listed in the recall are most at risk.
Check for the yellow striped tubing with an anti-siphon valve. The product uses catalog numbers 30893 or 30893-07. The sets are used for PCEA administration and cannot be primed by gravity.
Look for catalog numbers 30893 or 30893-07 on the administration set.
Replace the affected set with a new one that has no leak risk.
The PCEA ASV Yellow Microbore administration sets can leak between the male luer lock and yellow tubing, which may cause medication contamination or improper delivery.
Check for catalog numbers 30893 or 30893-07 on the administration set, which has yellow striped tubing and an anti-siphon valve.
The recall does not specify a stop-use instruction, but the product should be replaced to avoid potential leaks.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0386-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0386-2019 from Becton Dickinson. 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.
