Z-1075-2020 Class II Terminated

Recalled by Centurion Medical Products Corporation — Williamston, MI

FDA device recall Z-1075-2020 was initiated by Centurion Medical Products Corporation on Dec 11, 2019 and is designated Class II. Reason for recall: Incomplete seals on the sterile package may compromise the sterility The recall status is terminated (terminated Sep 4, 2020).

Recall Details

Product Type
Devices
Report Date
Feb 12, 2020
Initiation Date
Dec 11, 2019
Termination Date
Sep 4, 2020
Voluntary/Mandated
Voluntary: Firm initiated

Product Description

Centurion-Suture Tray DYNDR1210A SUTURING TRAY

Reason for Recall

Incomplete seals on the sterile package may compromise the sterility

Distribution Pattern

Nationwide Foreign: GHANA

Code Information

Product-Lot Code: DYNDR1210A SUTURING TRAY 2019031290

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1075-2020
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.