Becton Dickinson recalls Bard Mypicc Kit 5F Triple-Lumen (Catalog CK000278) due to supplier's surgical gown recall. Affected units include specific lot numbers 19FBN919 and 19GBZ466.
The kits contain surgical gowns which were subject to a recall by the supplier.
Becton Dickinson is recalling Bard MYPICC Kit 5: Triple-Lumen surgical kits because the surgical gowns they contain were previously recalled by the supplier. This means the kits may have unsafe gowns that could pose risks if used in medical settings.
The surgical gowns in these kits were previously recalled by the supplier due to potential safety issues. While the exact hazard isn't specified in this recall, the supplier's prior recall suggests the gowns might not meet safety standards for medical use.
Medical professionals using the Bard MYPICC Kit 5F Triple-Lumen surgical kits with specific lot numbers 19FBN919 and 19GBZ466 are most at risk. The recall affects hospitals and clinics that use these kits for surgical procedures.
Check for the catalog number CK000278 and lot numbers 19FBN919 or 19GBZ466 on the kit packaging. The kits are sold by Becton Dickinson & Company for medical use.
Look for lot numbers 19FBN919 or 19GBZ466 on the Bard MYPICC Kit 5F Triple-Lumen packaging.
The surgical gowns in these kits were previously recalled by the supplier due to potential safety issues.
Check the lot numbers on the packaging. If they match 19FBN919 or 19GBZ466, contact Becton Dickinson for guidance.
The recall is due to the supplier's prior recall of surgical gowns, but the specific hazard isn't detailed in this notice.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2079-2020 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2079-2020 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.
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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.
