MAUDE Adverse Event Report: SYNTHES GMBH SPEED 9X10X10MM IMPLANT; STAPLE, FIXATION, BONE

Model Number	SE-0910
Medical Device Problem Code	Manufacturing, Packaging or Shipping Problem (2975)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/31/2022
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.Device available for evaluation: complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.Initial reporter occupation: is a synthes employee.The investigation could not be completed; no conclusion could be drawn, as no product was received.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Review of the device history record(s) showed that there were no issues during the manufacture of this product, and any sub-components, which would contribute to this complaint condition.Part # se-0910.Synthes lot # mse210240.Supplier lot # mse210240.Release to warehouse date: (b)(6) 2022.Supplier: millstone medical.No ncrs were generated during production.The product was returned to depuy synthes for evaluation.The depuy synthes team conducted a visual inspection of the returned device.Visual analysis of the returned sample revealed that speed compression implant kit 09x10x10mm.It was confirmed that the 13mm drill guide instead of a 09mm was packaged with the product se-0910 in a speed compression implant kit 09x10x10mm box.A dimensional inspection for the peed compression implant kit 09x10x10mm was unable to be performed due to basic dimension are irrelevant to reported condition.As part of depuy synthes quality process, all devices are manufactured, inspected, and released to approved specifications.The overall complaint was confirmed for the peed compression implant kit 09x10x10mm.The root cause of the complaint condition can be confirmed due to the manufacturing issue.The received condition of the peed compression implant kit 09x10x10mm confirmed that the the 13mm drill guide instead of a 09mm was packaged with the product product se-0910 in a peed compression implant kit 09x10x10mm box.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
It was reported that during incoming inspection on (b)(6) 2022, the implant kits were found to contain drill guides for 13mm cci implants, and not for the 9mm cci implant that is packaged.There was no patient interaction, no patient consequence.No further information is available.This report is for a speed 9x10x10mm implant.This is report 1 of 2 for (b)(4).
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.H3, h6: part # se-0910, synthes lot # mse210240, supplier lot # mse210240, release to warehouse date: 24 aug 2022, supplier: (b)(4), no ncrs were generated during production.Review of the device history record(s) showed that there were no issues during the manufacture of this product, and any sub-components, which would contribute to this complaint condition.The product was returned to depuy synthes for evaluation.The depuy synthes team conducted a visual inspection of the returned device.Visual analysis of the returned sample revealed that speed compression implant kit 09x10x10mm.It was confirmed that the 13mm drill guide instead of a 09mm was packaged with the product se-0910 in a speed compression implant kit 09x10x10mm box.A dimensional inspection for the peed compression implant kit 09x10x10mm was unable to be performed due to basic dimension are irrelevant to reported condition.As part of depuy synthes quality process, all devices are manufactured, inspected, and released to approved specifications.The overall complaint was confirmed for the peed compression implant kit 09x10x10mm.The root cause of the complaint condition can be confirmed due to the manufacturing issue.The received condition of the peed compression implant kit 09x10x10mm confirmed that the 13mm drill guide instead of a 09mm was packaged with the product se-0910 in a peed compression implant kit 09x10x10mm box.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: SPEED 9X10X10MM IMPLANT
• Common Device Name: STAPLE, FIXATION, BONE
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): MONUMENT; 1101 synthes avenue; monument CO 80132
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA 19380 ; 3035526892
• MDR Report Key: 15508529
• Report Number: 8030965-2022-07545
• Device Sequence Number: 5171479
• Product Code: JDR
• UDI-Device Identifier: 00810633020111
• UDI-Public: (01)00810633020111
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K142292
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup

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: SE-0910
• Device Catalogue Number: SE-0910
• Device Lot Number: MSE210240
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/19/2022
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 08/31/2022
• Supplement Date Received by Manufacturer: 10/03/2022
• Initial Report FDA Received Date: 09/29/2022
• Supplement Report FDA Received Date: 10/24/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 08/19/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown