MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; DRESSING,HONEY,THERAHONEY,1.5 OZ TUBE

Catalog Number	MNK0015
Medical Device Problem Code	Device Ingredient or Reagent Problem (2910)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/12/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "turning out to be crystallized".
Additional Manufacturer Narrative
Customer reported issue of crystalization with item mnk0015 dressing,honey,therahoney,1.5 oz tube.The sample sent in for investigation was evaluated and was found to exhibit abnormal color, consistency, and pressure in the tube.The crystallization issue was not able to be confirmed with the sample sent in for investigation.The cause code was updated to reflect dc: supplier error non-asia (medline brnd), and the complaint was ok to close with no change to the reportability decision associated with this complaint.There were no reports of death, serious injury, medical intervention, or follow up care.It has been determined that the reported event could cause or contribute to serious injury if it were to occur again.In an abundance of caution, this is a reportable event.If additional information becomes available this report will be reopened and reevaluated.This medical device report (mdr) is being submitted as part of retrospective review activities, which include review of historical data in accordance with regulations at 21 cfr part 803.The information included in this mdr reflects the information reasonably known to the manufacturer at the time of this retrospective review and submission.

• Brand Name: MEDLINE
• Common Device Name: DRESSING,HONEY,THERAHONEY,1.5 OZ TUBE
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: felipe bifareti
• MDR Report Key: 50835142
• Report Number: 1417592-2026-45840
• Device Sequence Number: 10060330
• Product Code: FRO
• UDI-Device Identifier: 40884389154558
• UDI-Public: 40884389154558
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/20/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: MNK0015
• Device Lot Number: LMPTH0214B
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 06/19/2023
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/03/2023
• Initial Report FDA Received Date: 09/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown