DandleLION Kisses
Reason Microbial contamination
Product comes in a plastic bag which is labeled as follows recall
Recalled by Tarry Medical Products, Inc. · Danbury, CT, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Microorganism found inside vial.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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
Quantity: 46 cases (17664 vials)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot/Unit Numbers: DUP Manufacturer's Batch Code: F17272
Where it was sold
California Georgia Nebraska Ohio Pennsylvania Wisconsin
FDA's distribution note: Direct to PA, WI, OH, GA, NE, CA
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Tarry Medical Products, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 20, 2018
- In FDA report of
- Oct 24, 2018
- Terminated
- Nov 29, 2018
- FDA recall number
- F-0058-2019 · event 81082
- Official record
- FDA enforcement report search