MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP; THE SURGERY CENTER CATARACT

Catalog Number	VAL002CATSG
Medical Device Problem Code	Appropriate Device Problem Term/Code Not Available (3191)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	04/12/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
According to the customer, "moxifloxacin is placed in a med cup from the pack and drawing up in a tb syringe from the pack.A sterile disposable cannula is put on the syringe and the moxi is injected intracamerally.Once delivered fibers can be seen floating in the eye.Moxi is then flushed out of the eye and another dose is placed until no fibers are seen".It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.
Event or Problem Description
According to the customer, "moxifloxacin is placed in a med cup from the pack and drawing up in a tb syringe from the pack.A sterile disposable cannula is put on the syringe and the moxi is injected intracamerally.Once delivered fibers can be seen floating in the eye.Moxi is then flushed out of the eye and another dose is placed until no fibers are seen".

• Common Device Name: THE SURGERY CENTER CATARACT
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093 2753
• Manufacturer Contact: alex mathew ; three lakes drive; northfield, IL 60093-2753 ; 2249317042
• MDR Report Key: 19288744
• Report Number: 1423395-2024-00412
• Device Sequence Number: 18316183
• Product Code: OJK
• UDI-Device Identifier: 40195327250417
• UDI-Public: 40195327250417
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 05/10/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Catalogue Number: VAL002CATSG
• Device Lot Number: 24ABN973
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/12/2024
• Initial Report FDA Received Date: 05/10/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown