Becton Dickinson recalls PCEA Kit ASV Yellow Stripe Microbore (Catalog 10800177) due to potential leaks between male luer lock and tubing. Affected units include specific batch numbers.
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 Kit ASV Yellow Stripe Microbore tubing sets because they may leak between the connection point and the tubing. This leak risk could lead to contamination or improper medication delivery during IV therapy.
The tubing may leak between the male luer lock connection and the yellow-striped tubing. This leak could cause medication to escape from the system, potentially leading to contamination or incorrect dosing during IV therapy.
Healthcare professionals using the PCEA kit for intravenous therapy are most at risk. Patients receiving treatment with this specific tubing set may be affected if leaks occur.
Check for the yellow striped tubing with anti-siphon valve. The product uses catalog number 10800177 and includes specific batch numbers: 16127933, 17017602, 17055977, 17117153, 17125385, 18015788.
Verify the catalog number 10800177 and batch numbers listed in the recall notice.
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
Batch numbers 16127933, 17017602, 17055977, 17117153, 17125385, and 18015788.
The recall does not specify a stop-use instruction, but the product should be changed according to facility protocols or IV therapy guidelines.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0387-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0387-2019 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.
