DandleLION Kisses Recall: Microorganism Contamination Risk
Tarry Medical Products recalls DandleLION Kisses oral solution due to microorganism contamination. Check lot F17272 for details.
Stop using this now
Microorganism found inside vial.
Contact the company
What happened, in plain English
Tarry Medical Products, Inc. is recalling DandleLION Kisses Oral Use Only Single Patient Use vials because a microorganism was found inside the vial. The affected product contains 24% organic sucrose and is labeled for single application use. This recall covers 46 cases containing 17,664 vials distributed to Pennsylvania, Wisconsin, Ohio, Georgia, Nebraska, and California. Read more at govinfonow.com/recall/18650-dandlelion-kisses-recall-microorganism-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18650-dandlelion-kisses-recall-microorganism-contamination-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0058-2019
Cite this page
“DandleLION Kisses Recall: Microorganism Contamination Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18650-dandlelion-kisses-recall-microorganism-contamination-risk. Based on FDA recall #F-0058-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0058-2019%22&limit=1).
Why it’s dangerous
The presence of a microorganism inside the vial poses a contamination risk to the sterile oral solution. Using contaminated medical products can lead to infection or other adverse health effects, particularly in patients relying on single-use applications.
Who’s affected
Owners or users of DandleLION Kisses oral solution who purchased the product in plastic bags labeled for single patient use. Individuals using this specific medical sucrose solution are at risk due to potential contamination.
How to tell if you have this one
Look for plastic bags labeled "DandleLION MEDICAL DandleLION KISSES ORAL USE ONLY SINGLE PATIENT USE SINGLE APPLICATION 24% ORGANIC SUCROSE." Check the manufacturer's batch code, which is F17272, and the lot/unit number DUP. The product comes in a 2mL orange vial.
- Brand
DandleLION Medical- Category
Food
What to do — step by step
Stop using the product
Do not use any vials from the recalled batch due to the risk of microorganism contamination.
Check your lot number
Verify if your product has manufacturer's batch code F17272 and lot/unit number DUP.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “Direct to PA, WI, OH, GA, NE, CA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Georgia, Nebraska, Ohio, Pennsylvania, Wisconsin.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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 #F-0058-2019 (September 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0058-2019 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.