FDA Adverse Event Injury Summary report: N

LACTO 1.5 2X2 SQUARE PLATE

MDR report key: 23223415 · Received October 6, 2025

Report

Report Number
0001032347-2025-00401
Event Type
Injury
Date Received
October 6, 2025
Date of Event
September 5, 2025
Report Date
February 17, 2026
Manufacturer
BIOMET MICROFIXATION
Product Code
HRS
PMA / PMN Number
K955729
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. THE FOLLOWING SECTIONS WERE UPDATED: B4, B5, D4, G3, G6, H2, H3, H4, H6, H11 D4: POSSIBLE LOTS: 280480 65988363 65988363. POSSIBLE MANUFACTURING/EXPIRATION DATES: 280480 - MAR 10, 2021/MAR 10, 2026 65988363 - MAR 22, 2023/MAR 22, 2028 65988363 - MAR 22, 2023/MAR 22, 2028. POSSIBLE UDIS: (B)(4). THE REPORTED EVENT COULD NOT BE CONFIRMED DUE TO LACK OF PRODUCT/INFORMATION. NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. THE DEVICE HISTORY RECORD WAS REVIEWED AND NO DISCREPANCIES RELEVANT TO THE REPORTED EVENT WERE FOUND. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Additional Manufacturer Narrative · 0

(B)(4). D4: POSSIBLE LOTS: 280480 65988363 65988363 POSSIBLE EXPIRATION DATES: 280480 - MAR 10, 2026. 65988363 - UNK. 65988363 - UNK. POSSIBLE UDIS: (B)(4). (B)(4). - UNK. (B)(4). ¿ UNK. D6: UNKNOWN DATE IN (B)(6) 2025. D10: LACTO SCR 1.5X4MM 1.5 SYS 2PK CAT# 915-2315 LOT# 66204803. LACTO SCR 1.5X4MM 1.5 SYS 2PK CAT# 915-2315 LOT# 66303545. LACTO SCR 1.5X4MM 1.5 SYS 2PK CAT# 915-2315 LOT# 66239019. LACTO SCR 1.5X4MM 1.5 SYS 2PK CAT# 915-2315 LOT# 66307891. LACTO SCR 1.5X4MM 1.5 SYS 1PK CAT# 915-2315-EA LOT# 66619072. LACTO SCR 1.5X4MM 1.5 SYS 1PK CAT# 915-2315-EA LOT# 66619072. G2: JAPAN. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED.

Description of Event or Problem · 0

ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

Description of Event or Problem · 0

IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION PROCEDURE APPROXIMATELY 3 MONTHS POST IMPLANTATION DUE TO A PROTRUDING AND MIGRATED LACTOSORB PRODUCT THAT WAS CAUSING SWELLING AND REDNESS. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2574846 LACTO 1.5 2X2 SQUARE PLATE CRANIOFACIAL FIXATION PLATE, BIOABSORBABLE HRS BIOMET MICROFIXATION NI SEE ADD'L INFO

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Hospitalization| R SEE H11.