Carroll-Baccari recalls Wave Prep Tubes and single use cups due to Burkholderia cepacia contamination found in FDA-inspected samples. Consumers should stop using these products 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.
Carroll-Baccari is recalling Wave Prep Tubes and single-use cups because samples tested during an FDA inspection found them contaminated with Burkholderia cepacia. This contamination poses a health risk, so affected consumers should stop using the products.
Burkholderia cepacia is a type of bacteria that can cause serious infections, especially in people with weakened immune systems. The contamination was found in samples tested during an FDA inspection on October 15, 2019, indicating that the products were unsafe for consumption.
Anyone who owns or uses Carroll-Baccari Wave Prep Tubes (model 1710-03) or single-use cups (model 17--00-24) is affected. People with compromised immune systems are at higher risk due to the potential health effects of the bacteria.
Check for Wave Prep Tubes labeled 1710-03 or single-use cups labeled 17--00-24. These products were manufactured at Carroll-Baccari's facility and were sold in the United States.
Immediately stop using Wave Prep Tubes (1710-03) and single-use cups (17--00-24) as they contain harmful bacteria.
Burkholderia cepacia is a type of bacteria that can cause serious infections, especially in people with weakened immune systems.
The contamination was found during a Food and Drug Administration inspection on October 15, 2019, when samples of 114gm Lemon Prep tubes were tested.
Yes, Burkholderia cepacia can cause serious infections, particularly in individuals with compromised immune systems.
We’ve drafted a message you can send Carroll-Baccari to request your refund or repair — edit it as you like.
Subject: Recall Z-1551-2020 — Carroll-Baccari Carroll-Baccari Hello, I own a Carroll-Baccari that is covered by recall Z-1551-2020 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.
