MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; DBD-CATARACT PACK OCOTILLO

Catalog Number	LYN003CTOTA
Medical Device Problem Code	Unsealed Device Packaging (1444)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/02/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "the customer received a custom pack that was opened.".
Additional Manufacturer Narrative
The reported issue was open vendor seal; the customer received a custom pack that was opened.A photo of the completed pack was received for investigation, a physical sample was not received, finished good production records were reviewed, finished good pack build was reviewed, trending was reviewed, and a raw material stock check was completed with no defects found.The reported problem was confirmed by photo review, which found the seal near the tyvek was completely and cleanly opened across the base and the sides.This is considered mishandling as this was likely opened somewhere after the pack was initially built.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: DBD-CATARACT PACK OCOTILLO
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: azmat shah ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50234693
• Report Number: 1417592-2026-16595
• Device Sequence Number: 18710413
• Product Code: LRO
• UDI-Device Identifier: 40195327476718
• UDI-Public: 40195327476718
• Combination Product (Y/N): N
• Initial Reporter State: MT
• 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): 08/13/2026

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: LYN003CTOTA
• Device Lot Number: 23IBB131
• Was Device Available for Evaluation?: No
• 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: 01/02/2024
• Initial Report FDA Received Date: 08/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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