MAUDE Adverse Event Report: SMITH & NEPHEW, INC. Q-FIX ULTRA; SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Catalog Number	72205693
Medical Device Problem Code	Failure to Fire (2610)
Health Effect - Clinical Code	Perforation (2001)
Date of Event	08/25/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
H11: internal complaint reference: (b)(4).H3, h6: this complaint was opened by smith+nephew to document a product problem associated with a smith+nephew device.The reported problem relates to known inherent device and/or procedural risks that are appropriately documented in our risk files.Smith+nephew will continue to monitor trends in accordance with our post-market surveillance process and take necessary action as required if anticipated severity and/or occurrence rates are exceeded.Smith+nephew has no reason to suspect that the product failed to meet any specifications at the time of manufacture.Based on our review of all currently available information, we are unable to identify a definitive root cause.However, as the use of our product cannot be excluded as a potential cause or contributory factor to the reported issue, we are conservatively submitting this report in accordance with applicable regulations.If additional investigative findings or information becomes available that alters the conclusions of this report, a follow-up report will be submitted as required.
Event or Problem Description
It was reported that during an arthroscopy, four (4) q-fix ultra anchors could not deploy after insertion into the pre-drilled bone hole.The procedure was completed placing a s+n backup device into an additional drilled bone hole.There was a significant surgical delay greater than 30 minutes.No further complications were reported.
Additional Manufacturer Narrative
H2: corrected information in d4 (lot number removed and exp.Date should be read in blank) corrected information in h4 (mfg.Date should be read in blank).Additional information in h11.Devices and lot numbers involved with additional bone hole are: x1 part number: 72205693 and lot number: 2173656 (mfg.Date: 28-jan-2025, exp.Date: 28-jan-2028).X3 part number: 72205693 and lot number: 2176090 (mfg.Date: 22-feb-2025, exp.Date: 22-feb-2028).
Additional Manufacturer Narrative
H2: corrected information in h6 (component code, type of investigation & investigation findings).H3, h6: the reported device was not returned to the designated complaint unit for independent evaluation.However, an analysis of the customer provided image found three devices being held, the anchor is seen inside the insertion device.A review of device records showed there were no indications to suggest that the product did not meet manufacturing specifications upon release for distribution.A complaint history review found similar reported events.A risk management review found that the reported failure and/or harm was documented appropriately, and there were no indications to suggest the anticipated risk is not adequate.The root cause of the reported event could not be determined since findings cannot lead to a clear cause of the reported event.Factors that could have contributed to the reported event include (application of unintended inappropriate or excessive force to the device, attempted correction of a damaged device, or an impact event inconsistent with normal use).Based on this investigation, the need for corrective action is not indicated.

• Brand Name: Q-FIX ULTRA
• Common Device Name: SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 130 forbes blvd.; mansfield MA 02048
• Manufacturer (Section G): SMITH & NEPHEW, INC.; 130 forbes blvd.; mansfield MA 02048
• Manufacturer Contact: holly topping ; 1450 brooks rd.; memphis, TN 38116 ; 5123913905
• MDR Report Key: 23075511
• Report Number: 1219602-2025-02312
• Device Sequence Number: 9812598
• Product Code: GAT
• UDI-Device Identifier: 00885556890745
• UDI-Public: 885556890745
• Combination Product (Y/N): N
• Initial Reporter Country: SN
• PMA/510(K) Number: K232457
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 10/31/2025

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 Catalogue Number: 72205693
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/25/2025
• Supplement Date Received by Manufacturer: 10/02/2025; 10/29/2025
• Initial Report FDA Received Date: 09/17/2025
• Supplement Report FDA Received Date: 10/06/2025; 10/31/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 01/28/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown