MAUDE Adverse Event Report: SMITH & NEPHEW, INC. MICRPTR RGNSRB STR ANCHR W/1ULTRBRDSTRBL; FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE

Model Number	72204983
Medical Device Problem Code	Manufacturing, Packaging or Shipping Problem (2975)
Health Effect - Clinical Code	No Patient Involvement (2645)
Date of Event	10/08/2020
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the ce mark of the microraptor had been added on the packaging as a sticker.No case reported; therefore, there was no patient involvement.All available information has been disclosed.If additional information should become available, a supplemental report will be submitted accordingly.
Additional Manufacturer Narrative
Additional information received by the manufacturer has identified that this event should be re-evaluated for mdr reporting.The new information states that there is no malfunction of the device nor harm or patient injury, the labeling information on the package was aligned to the specification and it was reported in error, therefore, it was determined that this case does not meet the threshold for reporting and is a non-reportable event.

• Brand Name: MICRPTR RGNSRB STR ANCHR W/1ULTRBRDSTRBL
• Common Device Name: FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 130 forbes blvd.; mansfield MA 02048
• MDR Report Key: 10758899
• Report Number: 1219602-2020-01694
• Device Sequence Number: 3773116
• Product Code: MAI
• UDI-Device Identifier: 00885556710302
• UDI-Public: 00885556710302
• Combination Product (Y/N): N
• Initial Reporter Country: BE
• PMA/510(K) Number: K180361
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 11/05/2020

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: 72204983
• Device Catalogue Number: 72204983
• Device Lot Number: 50853838
• Was Device Available for Evaluation?: Yes
• Initial Date Received by Manufacturer: 10/08/2020
• Supplement Date Received by Manufacturer: 10/16/2020
• Initial Report FDA Received Date: 10/29/2020
• Supplement Report FDA Received Date: 11/05/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1