Medline recalls BARD MYPICC Kit (REF CK000095B) due to potential unsterilized cases. This affects vascular access kits sold between 2018-2019. Contact Medline for details.
One of the cases of product might not have been sterilized.
Medline is recalling BARD MYPICC Kits that might not have been properly sterilized. This could lead to infections during medical procedures if the kit is used without proper sterilization.
The recall is for cases that might not have been sterilized properly. If the kit isn't sterile, it could cause infections during medical procedures. This is a potential risk but not a direct hazard in normal use.
Healthcare professionals using vascular access kits for medical procedures. Patients receiving these kits are at risk if the kit wasn't properly sterilized.
Check for the product name 'BARD MYPICC Kit', reference number CK000095B, and the lot number 17YM5936. The kits were sold in cases of 5, packaged as sterile for vascular access procedures.
Verify if the case was sterilized by checking the lot number 17YM5936 and expiration date 04/30/2019.
The recall indicates potential unsterilized cases, so it's not safe to use without verification.
The recall doesn't specify a remedy, so contact Medline directly for guidance.
Look for the product name 'BARD MYPICC Kit', reference CK000095B, and lot number 17YM5936.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2378-2018 — Medline Medline Hello, I own a Medline that is covered by recall Z-2378-2018 from Medline. 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.
