Recall archive / FDA device enforcement
Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAM, Pack Number DYNDH1446A; 2) ARTHROGRA... — FDA record Z-2776-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Apr 8, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Centurion procedure packs, containing Caina syringes, labeled as: 1) ARTHROGRAM, Pack Number DYNDH1446A; 2) ARTHROGRAM TRAY, Pack Number MNS11965A; 3) ARTHROGRAPH TRAY, Pack Number MNS12670A; 4) BREAST BIOPSY KIT, Pack Number DYNDH1512; 5) CIRCUMCISION KIT, Pack Number CIT6535; 6) CIRCUMCISION KIT, Pack Number CIT7095; 7) CIRCUMCISION TRAY, Pack Number CIT7020; 8) CIRCUMCISION TRAY, Pack Number CIT6720; 9) CIRCUMCISION TRAY, Pack Number CIT6715; 10) CIRCUMCISION TRAY, Pack Number CIT7210; 11) CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6925; 12) DISPOSABLE NICU UMBILICAL INSERTION TRAY, Pack Number UVT1030; 13) MEDICAL CIRCUMCISION TRAY, Pack Number CIT6780; 14) NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6920; 15) NURSERY CIRCUMCISION TRAY, Pack Number CIT4845; 16) PUNCH BIOPSY KIT, Pack Number MNS8245; 17) RETINAL INJECTION KIT, Pack Number MNS12465; 18) STERILE 1CC SYR W/ 27GX1/2 NDL, Pack Number 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.
- Classification
- Class II
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- Not supplied
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2776-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | DYNDH1446A, Lot Number 2020102990; MNS11965A, Lot Number 2021061190; MNS11965A, Lot Number 2021072690; MNS11965A, Lot Number 2021083090; MNS11965A, Lot Number 2022041390; MNS11965A, Lot Number 2022091490; MNS11965A, Lot Number 2023041090; MNS12670A, Lot Number 2023060290; DYNDH1512, Lot Number 2021100490; CIT7095, Lot Number 2021061190; CIT6535, Lot Number 2024031880; CIT7020, Lot Number 2021120990; CIT6720, Lot Number 2022032290; CIT6715, Lot Number 2022062290; CIT7210, Lot Number 2022071990; CIT7020, Lot Number 2022091490; CIT7210, Lot Number 2022120590; CIT6715, Lot Number 2023012490; CIT7020, Lot Number 2023030290; CIT7210, Lot Number 2023030990; CIT7210, Lot Number 2023060290; CIT6925, Lot Number 2021081190; CIT6925, Lot Number 2021090290; CIT6925, Lot Number 2022070590; UVT1030, Lot Number 2021072190; UVT1030, Lot Number 2022032290; CIT6780, Lot Number 2021081650; CIT6780, Lot Number 2023092290; CIT6920, Lot Number 2024020290; CIT4845, Lot Number 2023042090; CIT4845, Lot Number 2023070390; CIT4845, Lot Number 2023081090; MNS8245, Lot Number 2022111890; MNS12465, Lot Number 2022072290; MNS12465, Lot Number 2022111890; MNS12465, Lot Number 2023042890; MNS12465, Lot Number 2023102390; MNS12465, Lot Number 2024022190; MNS12465, Lot Number 2024030790; MNS12465, Lot Number 2022022880; DYNDA2496, Lot Number 2023102590 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide distribution.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Sep 4, 2024
- Recall initiation date
- Apr 8, 2024
- Center classification date
- Aug 28, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.