FDA Device recall Z-2775-2024
Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAPH TRAY, Pack Name MNS12670A
- FDA Device
- Class II
- ongoing
- Published 2024-09-04
On 2024-09-04 the FDA classified a Class II recall of Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAPH TRAY, Pack Name MNS12670A by Medline Industries Northfield, citing medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that m….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2775-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-08 |
| Published | 2024-09-04 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | n/a |
Product
Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAPH TRAY, Pack Name MNS12670A; 2) BREAST BIOPSY KIT, Pack Name DYNDH1512A; 3) CIRCUMCISION TRAY, Pack Name CIT6720; 4) CIRCUMCISION TRAY, Pack Name CIT6715; 5) CIRCUMCISION TRAY, Pack Name CIT7020; 6) CIRCUMCISION TRAY, Pack Name DYNDA2271; 7) NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack Name CIT6920; 8) NURSERY CIRCUMCISION TRAY, Pack Name CIT4845; 9) PUNCH BIOPSY KIT, Pack Name MNS8245; 10) STERILE 1CC SYR W/ 27GX1/2 NDL, Pack Name DYNDA2496
Reason
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Identifiers
| code_info | MNS12670A, Lot Number 2022011090; MNS12670A, Lot Number 2022070690; MNS12670A, Lot Number 2023022190; MNS12670A, Lot…MNS12670A, Lot Number 2022011090; MNS12670A, Lot Number 2022070690; MNS12670A, Lot Number 2023022190; MNS12670A, Lot Number 2023101890; MNS12670A, Lot Number 2024021590; DYNDH1512A, Lot Number 2022121990; DYNDH1512A, Lot Number 2023101890; CIT6720, Lot Number 2021061490; CIT6715, Lot Number 2022100490; CIT7020, Lot Number 2023010690; DYNDA2271, Lot Number 2023022190; CIT6715, Lot Number 2023082290; CIT7020, Lot Number 2023101890; CIT6715, Lot Number 2023102090; CIT6715, Lot Number 2023120590; CIT6920, Lot Number 2021082390; CIT4845, Lot Number 2021122150; CIT4845, Lot Number 2022052450; MNS8245, Lot Number 2023082490; DYNDA2496, Lot Number 2023012790 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2775-2024%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.