MAUDE Adverse Event Report: Oscor Inc. Destino¿ Twist¿ Steerable Guiding Sheath; INTRODUCER, CATHETER

Model Number	DST0655509
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Codes	Hemorrhage/Blood Loss/Bleeding (1888); Fibrosis (3167); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/26/2026
Type of Reportable Event	Malfunction

• Brand Name: Destino¿ Twist¿ Steerable Guiding Sheath
• Common Device Name: INTRODUCER, CATHETER
• Manufacturer (Section D): Oscor Inc.; 4875 palm harbor blvd.; palm harbor FL 34683
• Manufacturer (Section G): Oscor Inc.; 4875 palm harbor blvd.; palm harbor FL 34683
• Manufacturer Contact: mohit malkani ; 4875 palm harbor blvd.; palm harbor, FL 34683 ; +1(727)937-2511
• MDR Report Key: 50302999
• Report Number: 1035166-2026-00068
• Device Sequence Number: 21508044
• Product Code: DYB
• UDI-Device Identifier: 00885672004019
• UDI-Public: 00885672004019
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K140406
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/18/2026

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
• Operator of Device: Health Professional
• Device Model Number: DST0655509
• Device Catalogue Number: DST0655509
• Device Lot Number: S10721753
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 08/17/2026
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 07/21/2026
• Supplement Date Received by Manufacturer: 08/17/2026
• Initial Report FDA Received Date: 08/18/2026
• Supplement Report FDA Received Date: 09/18/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/01/2026
• 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
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown