Carroll-Baccari recalls Pedia Prep 4 oz tubes and single-use cups that may be contaminated with Burholderia cepacia. Affected units were sold from 2021-2022. Consumers should contact Carroll-Baccari for details.
Product has the potential to be contaminated with Burholderia cepacia.
Carroll-Baccari is recalling Pedia Prep 4 oz tubes and single-use cups because they may be contaminated with Burholderia cepacia. This bacteria can cause infections, especially in people with weakened immune systems or medical devices.
Burholderia cepacia is a bacteria that can cause infections in people with medical devices or compromised immune systems. The product may be contaminated during manufacturing, leading to potential infections if used.
People using Pedia Prep for EKG/ECG recordings, especially those with medical devices or weakened immune systems. Most users are likely healthy adults or children.
Check for Pedia Prep 4 oz tubes (MD0033T) or single-use cups (MD0033-SUP) with serial numbers 29769, 29915, 30067, 30643 for tubes or 29770, 30027, 30049, 30711 for cups. These were sold from 2021-2022.
Look for serial numbers on the tubes or cups: MD0033T has 29769, 29915, 30067, 30643; MD0033-SUP has 29770, 30027, 30049, 30711.
Reach out to Carroll-Baccari for instructions on how to return or dispose of the product safely.
Burholderia cepacia is a bacteria that can cause infections in people with medical devices or weakened immune systems.
Check for Pedia Prep 4 oz tubes (MD0033T) with serial numbers 29769, 29915, 30067, 30643 or single-use cups (MD0033-SUP) with serial numbers 29770, 30027, 30049, 30711.
The recall states the product may be contaminated with Burholderia cepacia, which can cause infections in vulnerable individuals, but the risk is not described as causing serious injury in normal use.
We’ve drafted a message you can send Carroll-Baccari to request your refund or repair — edit it as you like.
Subject: Recall Z-0369-2020 — Carroll-Baccari Carroll-Baccari Hello, I own a Carroll-Baccari that is covered by recall Z-0369-2020 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.
