Device recall: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP)
Class II FDA enforcement event 84587. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
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.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Carroll-Baccari, Inc. started this device recall on 23 Dec 2019. The firm address in the FDA record is in Riviera Beach, FL. FDA put the recall in Class II. FDA event 84587 has 4 product records. The first FDA enforcement report date is 1 Apr 2020. The record gives the status Terminated, with the termination date 28 Sep 2021.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Nationwide, Canada, UK, Spain, Australia
Recalling firm
Carroll-Baccari, Inc., Riviera Beach, FL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
4 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1548-2020 | LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) | 8030 units | Class II | Terminated | 1 Apr 2020 |
| Z-1549-2020 | PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) | 850 units | Class II | Terminated | 1 Apr 2020 |
| Z-1550-2020 | MVAP MEDICAL SUPPLIES INC, Mavidon CardioPrep Single, 24 use cups, Re order # MCP-24 | 240 units | Class II | Terminated | 1 Apr 2020 |
| Z-1551-2020 | Wave Prep Tubes (1710-03) and single use cups (17--00-24) | 1444 units | Class II | Terminated | 1 Apr 2020 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2019
- 968
- Share of these events in Class II
- 88%
- Product records in this event
- 4Median of the firm: 4
- Events of the firm on the register
- 2
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 5 Sep 2019 | Lemon Prep: MD0019T - 4 oz tubes MD0019--SUP - Single Use Cups Skin preparation used to enhance signal quality of patien | Device | Class II | 2 |
Official channels
- FDA enforcement report Z-1548-2020The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 84587. https://recallregister.com/fda/ii/84587/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Nationwide, Canada, UK, Spain, Australia
- What quantity of product is in FDA event 84587?
- The event has 4 product records. The first record gives this quantity:
8030 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2019 have the same class?
- 88% of the 968 device events that started in 2019 are in Class II.