FDA Device recall Z-1090-2020
Centurion- Skin Prep Kits SB1280 SKIN SCRUB KIT SB1525 VAGINAL PREP TRAY
- FDA Device
- Class II
- terminated
- Published 2020-02-12
On 2020-02-12 the FDA classified a Class II recall of Centurion- Skin Prep Kits SB1280 SKIN SCRUB KIT SB1525 VAGINAL PREP TRAY by Centurion Medical Products, citing incomplete seals on the sterile package may compromise the sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1090-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-11 |
| Published | 2020-02-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Centurion Medical Products |
| Distribution | US |
Product
Centurion- Skin Prep Kits SB1280 SKIN SCRUB KIT SB1525 VAGINAL PREP TRAY
Reason
Incomplete seals on the sterile package may compromise the sterility
Identifiers
| code_info | Product/Description/Lot Numbers: SB1280 SKIN SCRUB KIT 2018112690 SB1525 VAGINAL PREP TRAY 2018103190 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Centurion Medical Products
- Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium Heparin Tubes (BD Vacutainer-BD Codes 367884 & 367960
FDA Device · Class II · 2020-07-15 · Centurion Medical Products - Centurion-Surgical trays DYNJ04079Z CIRCUMCISION TRAY STERILE DYNJ08835 DEBRIDEMENT TRAY W/SAFETY SCAL DYNJ1000 NEWBORN CIRCUMCISION TRAY
FDA Device · Class II · 2020-02-12 · Centurion Medical Products - Centurion-Skin Prep Tray DYNDP1015 SKIN PREP TRAY
FDA Device · Class II · 2020-02-12 · Centurion Medical Products - Centurion- Nasal Speculum NSP500ST STERILE NASAL SPECULUM
FDA Device · Class II · 2020-02-12 · Centurion Medical Products - Centurion-Incision /Drainage Tray ID1235A ESKENAZI INCISION & DRAINAGE TRAY ID1525 INCISION & DRAINAGE TRAY ID1670 I&D TRAY ID1715 INCISION…
FDA Device · Class II · 2020-02-12 · Centurion Medical Products
All Centurion Medical Products recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1090-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.