DandleLION Medical Product (Tarry Medical) – microorganism contamination (2018)
Class II: 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
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Product comes in a plastic bag which is labeled as follows: DandleLION MEDICAL DandleLION KISSES ORAL USE ONLY SINGLE PATIENT USE SINGLE APPLICATION 24% ORGANIC SUCROSE, D-12442 2mL; The Product Case Labeling is as follows: DandleLION MEDICAL D 12242 C384 DandleLION KISSES (2ML) 24% ORGANIC SUCROSE SOLUTION ORANGE VIAL QTY - 384
Brand
Tarry Medical Products, Inc.
Lot Codes / Batch Numbers
Lot/Unit Numbers: DUP Manufacturer's Batch Code: F17272
Products Sold
Lot/Unit Numbers: DUP Manufacturer's Batch Code: F17272
Tarry Medical Products, Inc. is recalling Product comes in a plastic bag which is labeled as follows: DandleLION MEDICAL DandleLION KISSES ORA due to Microorganism found inside vial.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Microorganism found inside vial.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, GA, NE, OH, PA, WI
Page updated: Jan 6, 2026