FDA Adverse Event Malfunction Summary report: N

DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG

MDR report key: 7391941 · Received April 3, 2018

Report

Report Number
3003898360-2018-00240
Event Type
Malfunction
Date Received
April 3, 2018
Date of Event
March 27, 2018
Report Date
March 27, 2018
Manufacturer
TELEFLEX MEDICAL
Product Code
GDG
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

(B)(4). PER DHR THE PRODUCT DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG # (B)(4) WAS MANUFACTURED ON 07/24/2017 A TOTAL OF (B)(4) PIECES. LOT WAS RELEASED ON 08/04/2017. DHR INVESTIGATION DID NOT SHOW ISSUES RELATED TO COMPLAINT. THE CUSTOMER RETURNED ONE REPRESENTATIVE SAMPLE OF (B)(4) DURAHOOK 1/4 HOOK 10 PKG/BOX 6 HKS/PKG FOR INVESTIGATION. THE ACTUAL SAMPLE WAS NOT RETURNED. THE RETURNED SAMPLE WAS VISUALLY EXAMINED WITH AND WITHOUT MAGNIFICATION. VISUAL EXAMINATION REVEALED THAT THERE ARE MULTIPLE BANDS THAT SHOWED SIGNS OF DISCOLORATION. THE DISCOLORATION OF THE BANDS IS A SIGN THAT THE BANDS HAD OVER-EXPOSURE TO HEAT AND/OR UV LIGHTING. (B)(4). A FUNCTIONAL TEST WAS CONDUCTED TO TEST THE DURABILITY OF THE RETURNED SAMPLE. ALL SIX DURAHOOKS WERE TESTED. THE DURAHOOK WAS ATTACHED TO A FORCE GAUGE VIA THE THERMOPLASTIC ELASTOMETRIC (TPE) BAND AND STRETCHED TO MEASURE THE AMOUNT OF FORCE ON THE BAND. THE TESTED DURAHOOKS YIELDED THE FOLLOWING RESULTS: OTHER REMARKS: 1ST TPE BAND: 3.31 LB-FORCE WITHOUT SNAPPING. 2ND TPE BAND: 3.06 LB-FORCE WITHOUT SNAPPING. 3RD TPE BAND: 3.47 LB-FORCE WITHOUT SNAPPING. 4TH TPE BAND: 3.58 LB-FORCE WITHOUT SNAPPING. 5TH TPE BAND: 3.32 LB-FORCE WITHOUT SNAPPING. 6TH TPE BAND: 3.28 LB-FORCE WITHOUT SNAPPING. NONE OF THE TESTED SAMPLES BROKE. ACCORDING TO DHF D001915, "THE BAND SHALL BE ABLE TO STRETCH TO AT LEAST DOUBLE OR 200% ITS ORIGINAL LENGTH WITH A FORCE OF 0.79 ¿ 0.15 LB-FORCE" AND "AT LEAST TRIPLE OR 300% ITS ORIGINAL LENGTH WITH A FORCE OF 0.90 ¿ 0.17 WITHOUT BREAKING." ALL SAMPLES WERE ABLE TO WITHSTAND AT LEAST 3.06 LB-FORCE WITHOUT BREAKING WHICH FAR EXCEEDS THE REQUIREMENT. NO FUNCTIONAL ISSUES WERE FOUND WITH THE RETURNED SAMPLES. SPECIFICATIONS PER GRAPHIC 14-2-001470 REV. 01 AND THE DHF FOR THIS PRODUCT, D001915 REV. 03, WERE REVIEWED AS A PART OF THIS COMPLAINT INVESTIGATION. A CORRECTIVE ACTION IS NOT REQUIRED AT THIS TIME SINCE NO FUNCTIONAL DEFECTS WERE FOUND WITH THE RETURNED SAMPLE. ONE REPRESENTATIVE SAMPLE WAS RETURNED. THE ACTUAL SAMPLE WAS NOT RETURNED. THE REPORTED COMPLAINT OF "BRITTLE/BREAKING" WAS NOT CONFIRMED BASED UPON THE SAMPLES RECEIVED. ONE REPRESENTATIVE SAMPLE WAS RETURNED, BUT THE ACTUAL SAMPLE WAS NOT. MULTIPLE BANDS SHOWED SIGNS OF DISCOLORATION WHICH INDICATES THAT THE SAMPLE WAS OVER-EXPOSED TO HEAT AND/OR UV LIGHTING. A FUNCTIONAL TEST WAS CONDUCTED TO TEST THE DURABILITY OF THE RETURNED SAMPLE. THE STRENGTH OF THE TPE BAND WAS TESTED VERSUS THE DESIGN SPEC AND ALL TESTED SAMPLES FAR EXCEEDED THE REQUIREMENT. A DEVICE HISTORY RECORD REVIEW WAS PERFORMED ON THE DEVICE WITH NO EVIDENCE TO SUGGEST A MANUFACTURING RELATED CAUSE. THERE WERE NO FUNCTIONAL ISSUES FOUND WITH THE RETURNED DURAHOOKS. SINCE ONLY A REPRESENTATIVE SAMPLE WAS RETURNED, THE ROOT CAUSE OF THIS COMPLAINT ISSUE COULD NOT BE DETERMINED.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE ELASTIC SEEMS TO BE BRITTLE AND/OR BREAKING. THERE WAS NO REPORTED PATIENT INJURY.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE HAS NOT BEEN RETURNED FOR INVESTIGATION. TELEFLEX WILL CONTINUE TO MONITOR AND TREND RELATED EVENTS.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE ELASTIC SEEMS TO BE BRITTLE AND/OR BREAKING. THERE WAS NO REPORTED PATIENT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
234101 DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG GDG TELEFLEX MEDICAL 73G1700265

Patients

Seq Age Sex Outcome Treatment
1