Carroll-Baccari recalls PediaPrep Tubes and Single use cups due to contamination with Burkholderia cepacia found in FDA samples. Affected products may pose health risks.
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.
Carroll-Baccari is recalling PediaPrep Tubes and Single-use cups because samples tested by the FDA found them contaminated with Burkholderia cepacia. This contamination could pose health risks to users.
Burkholderia cepacia is a type of bacteria that can cause infections, particularly in people with weakened immune systems. The contamination was found in samples collected during an FDA inspection in October 2019.
Parents or caregivers who use these products for infant formula preparation are most at risk. The recall covers all products made at Carroll-Baccari's facility.
Check for products labeled 'PediaPrep Tubes (MD0033-T)' or 'Single use cups (MD0033-SUP)'. All lots are affected by this recall.
Look for the product names and model numbers listed in the recall notice.
The recall notice states that samples were contaminated with Burkholderia cepacia, which can cause infections, especially in people with weakened immune systems. However, the exact health risks are not specified in the recall notice.
Check for products labeled 'PediaPrep Tubes (MD0033-T)' or 'Single use cups (MD0033-SUP)' as all lots are affected.
The recall notice does not specify any remedy or action steps beyond checking the product labels.
We’ve drafted a message you can send Carroll-Baccari to request your refund or repair — edit it as you like.
Subject: Recall Z-1549-2020 — Carroll-Baccari Carroll-Baccari Hello, I own a Carroll-Baccari that is covered by recall Z-1549-2020 from Carroll-Baccari. 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.
