Becton Dickinson recalls BARD MYPICC Kit 5F Triple-Lumen (Catalog CK000026A) due to supplier's surgical gown recall. Affected units include specific lot numbers. No action needed as the hazard is from a prior supplier recall.
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 with catalog number CK000026A because the surgical gowns inside were previously recalled by the supplier. This recall does not require immediate action for the consumer since the hazard comes from a prior supplier issue, not a defect in the current product.
The surgical gowns in these kits were previously recalled by the supplier due to a different issue. This means the gowns themselves were not defective but were part of a separate recall that the supplier handled. The hazard is not inherent to the current product but comes from the supplier's prior action.
Healthcare professionals using the BARD MYPICC Kit 5F Triple-Lumen surgical kits with specific lot numbers are likely affected. The risk is low as the hazard stems from a supplier recall, not a defect in the current product.
Check for the BARD MYPICC Kit 5F Triple-Lumen with catalog number CK000026A. Affected units have lot numbers 18JBU370, 18OB4147, or 19BBJ457.
Look for lot numbers 18JBU370, 18OB4147, or 19BBJ457 on the kit packaging.
No, the recall is due to a supplier's prior action on the gowns, not a defect in the current product. No action is needed.
Check the lot number on the kit packaging. If it matches 18JBU370, 18OB4147, or 19BBJ457, contact Becton Dickinson for guidance.
The hazard comes from a supplier's prior recall of the gowns, not a defect in the current product. The risk is low and no action is needed.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2076-2020 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2076-2020 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.
