MAUDE Adverse Event Report: ESTABLISHMENT LABS S.A. MOTIVA ERGONOMIX ROUND SILKSURFACE WITH QID; MOTIVA IMPLANTS

Catalog Number	ERSF-400Q
Medical Device Problem Code	Increased Sensitivity (2535)
Health Effect - Clinical Code	Discomfort (2330)
Type of Reportable Event	Serious Injury
Event or Problem Description
In (b)(6), patient had a breast augmentation using motiva implants.Started getting discomfort in the left breast, feeling tight, foreign, and firmer than the right.The right one felt natural and comfortable.After careful consideration and health problems, patient decided to get them out.When they were getting taken out, the left one was still intact however, it was the one that was causing discomfort in the first place.No patient demographics, such as age, weight, or ethnicity, were provided by the reporter, and no adverse outcomes for the patient have been noted.Efforts to gather additional information are ongoing, and the investigation remains in progress.
Additional Manufacturer Narrative
Palpability is a reason for complaints, and it is clearly characterized in the product dfu included with the implant, as stated above.The instructions for use in the directions for use were reviewed to determine if there are indications that ensure the prevention and good handling of the product.For this event, it is considered that the information is suitable on the section of surgical precautions as follows: ¿visibility and palpability of the implant can occur because the envelope is thin due to several causes, including excessive volume, the implant¿s content not being cohesive, or previous surgery and cutaneous aging.If the implant is fitted in a subglandular pocket, a change to a submuscular pocket is needed.The implant volume should be reduced, and it should be ensured that the content is a cohesive gel¿."unsatisfactory results such as wrinkling, asymmetry, implant displacement/ migration, incorrect size, implant palpability/visibility, scar deformity, and/or hypertrophic scarring, may occur.Some of these results may cause discomfort.Pre-existing asymmetry may not be entirely correctable by implant surgery.Revision surgery could be indicated to increase patient satisfaction, but this involves additional considerations and risks.Careful preoperative planning and surgical technique can minimize but not always prevent unsatisfactory results." also, a complete review of the dhr's was carried out, no deviation was found in the process, so it is established that there is no evidence of a relationship between the event and the manufacturing process.
Additional Manufacturer Narrative
A relationship between the reported events the device could not be established as the product was not returned for evaluation and due to lack of clinical evidence.A complete review of the dhr for lot involved was carried out, no deviation was found in the manufacturing process.Review of complaint history for the reported lot number and sterilization run found no other similar complaints reported in the past.A definitive root cause could not be determined.As no manufacturing, material or design issues were identified, no further investigation or additional actions are required at this time.Establishment labs will continue to monitor for similar complaints/trends.

• Brand Name: MOTIVA ERGONOMIX ROUND SILKSURFACE WITH QID
• Common Device Name: MOTIVA IMPLANTS
• Manufacturer (Section D): ESTABLISHMENT LABS S.A.; building b-25, coyol free zone; alajuela,alajuela
• Manufacturer (Section G): ESTABLISHMENT LABS S.A.; building b-25, coyol free zone; alajuela,alajuela
• Manufacturer Contact: susana hidalgo ; building b-25, coyol free zone; alajuela,alajuela ; 8003554164
• MDR Report Key: 21412283
• Report Number: 3012883202-2025-00384
• Device Sequence Number: 9518676
• Product Code: FTR
• UDI-Device Identifier: 07445161012388
• UDI-Public: (01)07445161012388(11)170522(17)220522
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/09/2025

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?: No
• Operator of Device: Health Professional
• Device Expiration Date: 05/22/2022
• Device Catalogue Number: ERSF-400Q
• Device Lot Number: 17050597
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/27/2025
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 02/19/2025
• Supplement Report FDA Received Date: 04/09/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/22/2017
• 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
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown