Lower riskMedical device recall · FDA · Published December 23, 2019
Carroll-Baccari LemonPrep Tubes and Cups Recall: Contamination Risk
Carroll-Baccari recalls LemonPrep Tubes and Single-use cups due to Burkholderia cepacia contamination found in FDA samples. Consumers should check product labels for model numbers MD0019-T or MD0019-SUP.
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.
Take action
Contact the company
📍Recalling firmCarroll-Baccari, Inc.6625 White Dr · Riviera Beach, FL 33407-1209
“Carroll-Baccari LemonPrep Tubes and Cups Recall: Contamination Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/66215-carroll-baccari-lemonprep-tubes-and-cups-recall-contamination-risk. Based on FDA recall #Z-1548-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1548-2020%22&limit=1).
The Food and Drug Administration announced on Dec. 23, 2019, that Carroll-Baccari, Inc. is recalling LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) due to contamination with Burkholderia cepacia. The agency said the recall covers all lots of the products.
How to tell if you have it
Brand: Carroll-Baccari
Product names: LemonPrep Tubes, Single use cups
Model numbers: MD0019-T, MD0019-SUP
Lot codes: All Lots
Units affected: 8030
The hazard
Samples of 114gm tubes of Lemon Prep collected during an FDA inspection on Oct. 15, 2019, were tested and found to be contaminated with Burkholderia cepacia, according to the FDA.
Context
GovInfoNow's records show Carroll-Baccari, Inc. has one other recall on record since Sept. 5, 2019: a Lemon Prep Tubes recall for potential Burholderia cepacia contamination issued on that date. Other recent recalls of similar products include Medline Convenience Kits Recall (June 12, 2026), Cardinal Health Presource Convenience Kits Recall (Aug. 10, 2026), and Medline Medical Kits Recalled Due to Possible Bacillus Contamination (June 11, 2026).
How to tell if you have this one
Check for model numbers MD0019-T on LemonPrep Tubes or MD0019-SUP on Single-use cups. The products were manufactured at Carroll-Baccari's facility and sold from the time of production until the recall was issued.
Brand
Carroll-Baccari
Category
Medical device
FDA recall event · 4 products
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
Nationwide, Canada, UK, Spain, Australia
Recall number
Product, codes & lots
Quantity
Z-1548-2020
LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP); All Lots
8030 units
Z-1549-2020
PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP); All Lots
850 units
Z-1550-2020
MVAP MEDICAL SUPPLIES INC, Mavidon CardioPrep Single, 24 use cups, Re order # MCP-24; All Lots
240 units
Z-1551-2020
Wave Prep Tubes (1710-03) and single use cups (17--00-24); All Lots
1444 units
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for model numbers MD0019-T on LemonPrep Tubes or MD0019-SUP on Single-use cups.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Nationwide, Canada, UK, Spain, Australia” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 21 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1548-2020 (December 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1548-2020 to see it in context.
Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.