LACTO 1.5 2X2 SQUARE PLATE
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
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.
(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.
ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
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. |