MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION PERI-STRIPS; MESH, SURGICAL

Catalog Number PSDA60ECH

Device Problem Disconnection (1171)

Patient Problem No Patient Involvement (2645)

Event Date 07/29/2020

Event Type  malfunction  

Manufacturer Narrative

(b)(6).Should additional relevant information become available, a supplemental report will be submitted.

Event Description

It was reported that the peri-strip did not adhere to the stapler; further described as ¿they did not allow it to dry off the stapler well enough¿.This was identified prior to use.There was no patient involvement.No additional information is available.

Manufacturer Narrative

H10: a batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot.The device was not received for evaluation; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.

• Brand Name: PERI-STRIPS
• Type of Device: MESH, SURGICAL
• Manufacturer (Section D): BAXTER HEALTHCARE CORPORATION; deerfield IL
• MDR Report Key: 10437630
• MDR Text Key: 203876965
• Report Number: 1416980-2020-05130
• Device Sequence Number: 1
• Product Code: FTM
• UDI-Device Identifier: 00085412658803
• UDI-Public: (01)00085412658803
• Combination Product (y/n): Y
• PMA/PMN Number: K192615
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,health
• Type of Report: Initial,Followup
• Report Date: 09/22/2020

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 Operator: Health Professional
• Device Expiration Date: 02/20/2021
• Device Catalogue Number: PSDA60ECH
• Device Lot Number: SP20E11-1450296
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 07/29/2020
• Initial Date FDA Received: 08/21/2020
• Supplement Dates Manufacturer Received: 09/11/2020
• Supplement Dates FDA Received: 09/22/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1