FDA Device recall Z-3024-2024
Medline Convenience kits labeled as: 1) PREP TRAY, Pack Number DYNDA1540
- FDA Device
- Class II
- ongoing
- Published 2024-09-18
On 2024-09-18 the FDA classified a Class II recall of Medline Convenience kits labeled as: 1) PREP TRAY, Pack Number DYNDA1540 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-3024-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-08 |
| Published | 2024-09-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | n/a |
Product
Medline Convenience kits labeled as: 1) PREP TRAY, Pack Number DYNDA1540; 2) STERILE PREP TRAY , Pack Number DYNDA2499; 3) ED PREP TRAY, Pack Number DYNDA2519; 4) ED PREP TRAY, Pack Number DYNDA2519H ; 5) PRE-OP PREP KIT , Pack Number DYNDA3076; 6) PILGRIM PREP TRAY , Pack Number DYNDC3282; 7) PILGRIM PREP TRAY , Pack Number DYNDC3282A ; 8) PILGRIM PREP TRAY , Pack Number DYNDC3282B ; 9) KYPHO PREP PACK-LF, Pack Number DYNJ0618280G ; 10) KYPHO PREP PACK-LF, Pack Number DYNJ0618280I ; 11) KYPHO PREP PACK-LF, Pack Number DYNJ0618280J ; 12) SPECIAL PROCEDURE PREP TRAY-LF, Pack Number DYNJ0738967A ; 13) BASIC SET UP PACK-LF, Pack Number DYNJ28988I ; 14) BASIC SET UP PACK-LF , Pack Number DYNJ28988I ; 15) VERTEBRALPLASTY PREP TRAY PACK, Pack Number DYNJ36311A ; 16) PK-SETUP PACK , Pack Number DYNJ43804A ; 17) SKIN LESION PACK, Pack Number DYNJ44258G ; 18) SETUP PACK, Pack Number DYNJ46187D ; 19) PK-SET UP -LF , Pack Number DYNJ53220B ; 20) IR PATIENT PREP KIT-LF, Pack Number DYNJ64857A ; 21) SKIN SCRUB PACK , Pack Number DYNJ68561; 22) DMEK PREP PACK, Pack Number DYNJ81659A ; 23) SET UP PACK , Pack Number DYNJ84247; 24) BASIC SET UP PACK-LF, Pack Number DYNJ85036; 25) SET UP CDS-ASC, Pack Number DYNJ900073C; 26) GENERAL SET UP, Pack Number DYNJ906282C; 27) JEWISH MAJOR SETUP, Pack Number DYNJ909261A; 28) SET UP, Pack Number DYNJ909403 ; 29) PREP TRAY , Pack Number DYNJRA1280A; 30) PREP TRAY , Pack Number DYNJRA1424 ; 31) NERVE BLOCK/W , Pack Number DYNJRA1424H; 32) PREP TRAY, Pack Number DYNJRA1498B; 33) PREP TRAY , Pack Number DYNJRA1583C; 34) PREP TRAY , Pack Number DYNJRA1760 ; 35) PREP TRAY , Pack Number DYNJRA1774 ; 36) PREP TRAY , Pack Number DYNJRA1783 ; 37) PREP TRAY , Pack Number DYNJRA1946A; 38) WINCHESTER PREP PACK-LF , Pack Number PHS627837003 ; 39) WINCHESTER PREP PACK-LF , Pack Number PHS627837003A
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 | DYNDA1540, Lot Number 23JBV995; DYNDA1540, Lot Number 23GBA155; DYNDA1540, Lot Number 23EBB508; DYNDA1540, Lot Numbe…DYNDA1540, Lot Number 23JBV995; DYNDA1540, Lot Number 23GBA155; DYNDA1540, Lot Number 23EBB508; DYNDA1540, Lot Number 22LBK096; DYNDA1540, Lot Number 22JBQ748; DYNDA1540, Lot Number 22HBC421; DYNDA1540, Lot Number 22DBP691; DYNDA1540, Lot Number 22ABU584; DYNDA1540, Lot Number 21BBI623; DYNDA1540, Lot Number 20LBU589; DYNDA1540, Lot Number 20KBL865; DYNDA1540, Lot Number 20JBP526; DYNDA1540, Lot Number 20IBD073; DYNDA1540, Lot Number 20HBT535; DYNDA1540, Lot Number 20HBQ630; DYNDA1540, Lot Number 20HBB154; DYNDA1540, Lot Number 2019050290; DYNDA1540, Lot Number 2019061890; DYNDA1540, Lot Number 2019071290; DYNDA2499, Lot Number 21JBI254 ; DYNDA2519, Lot Number 22FBC352 ; DYNDA2519H , Lot Number 22FBC352 ; DYNDA3076, Lot Number 24ABU746 ; DYNDC3282, Lot Number 23CLA266 ; DYNDC3282, Lot Number 23DLA289 ; DYNDC3282, Lot Number 23FLA594 ; DYNDC3282A , Lot Number 23HLA208 ; DYNDC3282A , Lot Number 23ILA470 ; DYNDC3282B , Lot Number 23LLA874 ; DYNDC3282B , Lot Nu |
|---|
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-3024-2024%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.