Becton Dickinson recalls MYPICC Kit 4F Single-Lumen (Catalog CK000276) due to supplier's surgical gown recall. Affected units include specific lot numbers. No action needed as the hazard is from a supplier recall.
The kits contain surgical gowns which were subject to a recall by the supplier.
Becton Dickinson is recalling their MYPICC Kit 4F Single-Lumen surgical kits because the surgical gowns inside were previously recalled by the supplier. This means the kits themselves aren't the problem, but the gowns were already part of a supplier recall.
The surgical gowns in the kits were previously recalled by the supplier due to a safety issue. This means the gowns themselves might not be safe, but the kits themselves are not defective.
Healthcare professionals using these kits for surgical procedures are likely affected. The risk is low since the hazard comes from a supplier recall, not a direct defect in the kits.
Check for the catalog number CK000276 on the kit. Affected lots include 18JBB605, 18KBZ117, 19EBE196, 19GBG860, 19SBH077, and 19UBA090.
Look for the lot numbers 18JBB605, 18KBZ117, 19EBE196, 19GBG860, 19SBH077, or 19UBA090 on the kit packaging.
No action is needed as the hazard comes from a supplier recall, not a defect in the kits themselves.
Check the lot number on the kit packaging. If it matches the affected lots, contact Becton Dickinson for guidance.
The kits themselves are not dangerous; the surgical gowns were previously recalled by the supplier.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2077-2020 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2077-2020 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.
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.
