MAUDE Adverse Event Report: AESCULAP AG CARBON STEEL SAFETY SCALPEL #23; DISPOSABLE SCALPELS

Model Number	BA823SU
Medical Device Problem Code	Tear, Rip or Hole in Device Packaging (2385)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/29/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Manufacturing site evaluation: investigation on-going.Additional information / investigation results will be provided in a supplemental report.This is a similar device report.The involved device is not marketed in the us.
Event or Problem Description
It was reported that there was an issue with ba823su - carbon steel safety scalpel #23.According to the complaint description, the primary packaging-torn.The packaging of the scalpel (primary packaging) tore, causing the equipment is not sterile.There was no described patient harm.Additional information was not provided nor available.The malfunction is filed under aag reference (b)(4).
Additional Manufacturer Narrative
Investigation results: leading device.Reference code (b)(4).Device name carbon steel safety scalpel #23.Serial number n/a.Batch number 4512049006.Manufacturing date 16.10.2020.Products are available for investigation.Failure description.One sample been sent for investigation and showed a damaged foil.Vigilance investigator carried out the pictorial documentation visually and microscopically.The sample is showing a rested part of the pe foil on the sealing area and the other part torn and loosened from the sealing area.As there is no hint for a material issue on the foil itself and due to tests performed during an earlier complaint (b)(4) which showed no deviation regarding the sealing, we therefore assume that there is no manufacturing issue.Batch history review.The device quality and manufacturing history records have been checked for the available lot number and were found to be according to our specifications valid at the time of production.There are no similar complaints against the same lot number with this error pattern.Explanation and rationale based on our investigation of the affected sample and the fact that in 5 years only two complaints from two different customers have been reported regarding this issue, we assume that there is no product deviation.Conclusion and root cause due to the current deviation and according to the explanation and rationale, the root cause of the problem is most probably usage-related.There is actually no hint regarding a manufacturing issue as the sealing boarders are existent and the sealing process is validated.A peel force measurement showed no deviation from the expectable force.Additionally, there are only complaints from two different customers regarding this issue in the last 5 years.Based upon the investigations results a capa is not necessary.

• Brand Name: CARBON STEEL SAFETY SCALPEL #23
• Common Device Name: DISPOSABLE SCALPELS
• Manufacturer (Section D): AESCULAP AG; po box 40; tuttlingen, 78501 ; GM 78501
• MDR Report Key: 11731525
• Report Number: 9610612-2021-00328
• Device Sequence Number: 19840322
• Product Code: GDX
• UDI-Device Identifier: 04046963510749
• UDI-Public: 4046963510749
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/02/2021

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 Expiration Date: 10/15/2025
• Device Model Number: BA823SU
• Device Catalogue Number: BA823SU
• Device Lot Number: 4512049006
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/19/2021
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/30/2021
• Supplement Date Received by Manufacturer: 08/11/2021
• Initial Report FDA Received Date: 04/27/2021
• Supplement Report FDA Received Date: 09/02/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1