FDA Device recall Z-1548-2020
LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP)
- FDA Device
- Class II
- terminated
- Published 2020-04-01
On 2020-04-01 the FDA classified a Class II recall of LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) by Carroll Baccari, citing 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 cep….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1548-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-23 |
| Published | 2020-04-01 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Carroll Baccari |
| Distribution | US |
Product
LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP)
Reason
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.
Identifiers
| code_info | All Lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1548-2020%22
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