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Carroll-Baccari, Inc. recalls Wave Prep Tubes (1710-03) and single use cups (17--00-24)
Recalled April 1, 2020 · FDA recall Z-1551-2020 · Carroll-Baccari
Hazard
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. · FDA Class II
Units
1444 units
Sold at
Nationwide, Canada, UK, Spain, Australia
Description
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.
Product
Wave Prep Tubes (1710-03) and single use cups (17--00-24)
Manufacturer(s)
Carroll-Baccari, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →