Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1548-2020 — LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP)

U.S. FDA — Device Enforcement · United States · 2019-12-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1548-2020
Date of alert
2019-12-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Carroll-Baccari, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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