Becton Dickinson recalls BARD MYPICC Kit : Supplier recalled surgical gowns in specific lots. No action needed as the hazard is from a supplier's prior recall.
The kits contain surgical gowns which were subject to a recall by the supplier.
Becton Dickinson is recalling BARD MYPICC Kit 5F Dual-Lumen with specific lot numbers due to a supplier's prior recall of surgical gowns. This does not pose a direct risk to users as the hazard comes from the supplier's action, not the product itself.
The hazard stems from the supplier recalling surgical gowns that were part of the kit. This means the gowns themselves were previously recalled by the supplier for a different reason, but the kit itself is not defective.
Users of the BARD MYPICC Kit 5F Dual-Lumen with lot numbers 19ABF426 or 19BBJ459 may be affected. Healthcare workers using the kit are most at risk if they have the recalled lot numbers.
Check the lot number on the BARD MYPICC Kit 5F Dual-Lumen packaging. The affected lots are 19ABF426 and 19BBJ459.
Look for lot numbers 19ABF426 or 19BBJ459 on the kit packaging.
No action is needed as the hazard comes from the supplier's prior recall, not a defect in the kit itself.
No action is required since the hazard is from the supplier's recall, not the product's defect.
The kit itself is not dangerous; the hazard is from the supplier's prior recall of surgical gowns, which does not affect the kit's safety.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2075-2020 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2075-2020 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.
