Mavidon is recalling 24-use CardioPrep cups due to contamination with Burkholderia cepacia found in FDA samples. Consumers should stop using these cups immediately.
Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug Administration inspection on October 15, 2019 were tested and found to be contaminated with Burkholderia cepacia. Mavidon is recalling all products manufactured at their facility.
Mavidon is recalling all CardioPrep Single 24-use cups because samples tested by the FDA found them contaminated with Burkholderia cepacia bacteria. This contamination could pose a health risk to users.
The cups were found contaminated with Burkholderia cepacia bacteria during an FDA inspection. This bacteria can cause serious infections, especially in individuals with weakened immune systems.
Users of Mavidon CardioPrep Single 24-use cups are affected. People with compromised immune systems or those using the product for medical purposes are at higher risk.
Check for Mavidon CardioPrep Single 24-use cups with reorder number MCP-24. The recall covers all lots manufactured at the facility.
Immediately stop using all Mavidon CardioPrep Single 24-use cups as they may be contaminated with Burkholderia cepacia.
FDA samples of 114gm Lemon Prep tubes found Burkholderia cepacia contamination, so Mavidon is recalling all products from their facility.
Check for Mavidon CardioPrep Single 24-use cups with reorder number MCP-24. The recall covers all lots manufactured at the facility.
Stop using the cups immediately and contact Mavidon for further instructions.
We’ve drafted a message you can send Mavidon to request your refund or repair — edit it as you like.
Subject: Recall Z-1550-2020 — Mavidon Mavidon Hello, I own a Mavidon that is covered by recall Z-1550-2020 from Mavidon. 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.
