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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: OSCOR INC. SAFESHEATH II INTRODUCER, CATHETER

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OSCOR INC. SAFESHEATH II INTRODUCER, CATHETER Back to Search Results
Model Number SS6
Device Problem Material Too Rigid or Stiff (1544)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 07/18/2019
Event Type  malfunction  
Manufacturer Narrative
The device was used for treatment. Two 6f safesheath ii introducer sheaths were returned from the customer without dilator. Both sheaths were already peeled apart by the customer upon receipt of the product. There were no other accessories. Traces of blood were found on and inside of both sheaths. The sheaths were reported from 2 different lots. Both sheaths were received in the same bag, so it is not possible to differentiate one lot from the other. On review of both the sheaths, the scorelines of the peeled sheaths were found to be normal and smooth. It was confirmed that the hemostatic valve in sheath split along half of its diameter and could not split apart completely. Break force test data was reviewed and showed that all data was within tolerance. Returned devices analysis reveals that hemostatic valves were torn and fatigued and the pegs of the introducers looked good. The exact root cause of seal not able to split remains inconclusive. The probable cause of this issue could be if the valve had not been seated properly on the pegs then the valve may slip out during peeling process. The event will be re-evaluated if additional information becomes available. Oscor will continue to monitor this event type. The device history records were reviewed to confirm that the device passed all applicable in-process and final inspections. Per procedure (adelante-s introducer sheath in process and final inspection). Qa performs inspection as per sampling plan ansi z 1. 4, special level 4, aql 0. 40 reduced. Break and peel test: using samples from fit check, manually break the sheath and hub and verify that the seal splits easily without extreme elongation. Also verify that the split cap and seal remain secure and do not break free or loosen from the sheath hub. Manually peel the sheath and verify the sheath peels easily along the sheath body and tip. Per ifu sharply snap the tabs of valve housing in a plane perpendicular to the long axis of the sheath to split the valve and peel sheath apart while withdrawing from the vessel. No further follow-up is required. Based on the investigation, a capa is not required as findings did not identify a design, labeling or manufacturing non-conformity. The event will be re-evaluated if additional information becomes available. Oscor will continue to monitor this event type and risk.
 
Event Description
It was reported that successful implant procedure of both device and leads. During implant procedure the physician experienced difficulty peeling the sheath. The enter part of the valve did not split. The gummy part and a small white plastic round part did not split and stayed on the lead during peeling away. The physician was able to cut away the parts that stayed around the lead without any issue. References of both 6f sheaths are dp08787 and dp09240. Lot number dp09240 will be addressed under mdr 1035166-2021-00094.
 
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Brand NameSAFESHEATH II
Type of DeviceINTRODUCER, CATHETER
Manufacturer (Section D)
OSCOR INC.
3816 desoto blvd.
palm harbor FL 34683 1816
Manufacturer (Section G)
OSCOR INC.
3816 desoto blvd.
palm harbor FL 34683 1816
Manufacturer Contact
doug myers
3816 desoto blvd.
palm harbor, FL 34683-1816
7279372511
MDR Report Key12422518
MDR Text Key270192314
Report Number1035166-2021-00093
Device Sequence Number1
Product Code DYB
UDI-Device Identifier20802526532447
UDI-Public20802526532447
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K122084
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor,foreign
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 09/03/2021
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received09/03/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator
Device Model NumberSS6
Device Catalogue NumberSS6
Device Lot NumberDP08787
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer01/20/2020
Is the Reporter a Health Professional?
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received09/01/2021
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured06/25/2018
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

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