MAUDE Adverse Event Report: SMITH & NEPHEW ORTHOPAEDICS AG TRIAL FEMORAL HEAD 32 S/+0; PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CEMENTED OR NON-POROUS

Model Number	75100850
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/01/1901
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that he fins of the trial head broke off intraoperatively and remained in the patient's body.The current state of health of the patient is unknown.
Additional Manufacturer Narrative
H3, h6: it was reported that the fins of overall 6 global femoral trial heads broke off intraoperatively and remained in the patient's body.The current state of health of the patient is unknown.The devices, which intent use is in treatment, were returned for investigation.The reported failure mode of "fracture" can be confirmed.One or more flags are broken off on every single trial head.A review of the batch record revealed no deviations from the standard manufacturing process, that could have contributed to the reported issue.A review of the risk management documentation verifies the failure mode and severity of the reported issue.For the batch in scope two further complaints were recorded, both of which were reported with this complaint.According to document "processing (cleaning, disinfection and sterilization) of instruments from smith & nephew orthopaedics ag" (lit.N°03389-en 1363 v3 11/19), all devices must be inspected and controlled for proper functioning after cleaning/disinfection.After the performed investigation we assume that the devices met specification at the time of manufacturing.Previous investigations demonstrated that the trial femoral head may disconnect from the stem taper intra-operatively and flaps might break off.In combination with our continuous effort to improve our products, evaluations aimed at optimizing this instrument have been initiated.The performance of the device is nonetheless within the risks, which are anticipated in the risk management documentation of the product, both in occurrence and severity.The continued performance of the device shall be monitored through standard post market surveillance review processes.The reported failure mode of a flap breakage can be confirmed.A relationship between device and reported event can be confirmed.The root cause is attributed to a insufficient design specification.S+n will continue to monitor these devices for similar issues.
Event or Problem Description
It was reported that 5 trial heads had an unspecified failure.Upon arrival, it was noticed that all of them had a broken fin.It is unknown when the failure occurred and if there was any patient involved.
Additional Manufacturer Narrative
Corrected information in: b1 and b4.Internal reference number: (b)(4).
Additional Manufacturer Narrative
It was reported that 5 trial heads had an unspecified failure.Upon arrival, it was noticed that all of them had a broken fin.It is unknown when the failure occurred and if there was any patient involved.The devices, which intent use is in treatment, were returned for investigation.The reported failure mode of "fracture" can be confirmed.One or more flags are broken off on every single trial head.A review of the batch record revealed no deviations from the standard manufacturing process, that could have contributed to the reported issue.A review of the risk management documentation verifies the failure mode and severity of the reported issue.For the batch in scope two further complaints were recorded, both of which were reported with this complaint.According to document "processing (cleaning, disinfection and sterilization) of instruments from smith & nephew orthopaedics ag" (lit.N°03389-en 1363 v3 11/19), all devices must be inspected and controlled for proper functioning after cleaning/disinfection.After the performed investigation we assume that the devices met specification at the time of manufacturing.Previous investigations demonstrated that the trial femoral head may disconnect from the stem taper intra-operatively and flaps might break off.In combination with our continuous effort to improve our products, evaluations aimed at optimizing this instrument have been initiated.The performance of the device is nonetheless within the risks, which are anticipated in the risk management documentation of the product, both in occurrence and severity.The continued performance of the device shall be monitored through standard post market surveillance review processes.The reported failure mode of a flap breakage can be confirmed.A relationship between device and reported event can be confirmed.The root cause is attributed to a insufficient design specification.S+n will continue to monitor these devices for similar issues.

• Brand Name: TRIAL FEMORAL HEAD 32 S/+0
• Common Device Name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CEMENTED OR NON-POROUS
• Manufacturer (Section D): SMITH & NEPHEW ORTHOPAEDICS AG; schachenallee 29; aarau CH-50 00; SZ CH-5000
• MDR Report Key: 11838283
• Report Number: 9613369-2021-00221
• Device Sequence Number: 17254142
• Product Code: LZO
• UDI-Device Identifier: 07611996121834
• UDI-Public: 07611996121834
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K132435
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 08/21/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 75100850
• Device Catalogue Number: 75100850
• Device Lot Number: A67276
• Was Device Available for Evaluation?: Yes
• Initial Date Received by Manufacturer: 04/29/2021
• Supplement Date Received by Manufacturer: 07/07/2021; 07/07/2021; 08/19/2021
• Initial Report FDA Received Date: 05/17/2021
• Supplement Report FDA Received Date: 07/08/2021; 08/06/2021; 08/21/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention