FDA Device recall Z-3061-2024

Medline Convenience kits, labeled as: aa1) BURN PACK-LF, Pack Number DYNJ0781678S

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: aa1) BURN PACK-LF, Pack Number DYNJ0781678S 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-3061-2024
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: aa1) BURN PACK-LF, Pack Number DYNJ0781678S ; 2) BURN PACK , Pack Number DYNJ0976092P ; 3) BURN PACK-LF, Pack Number DYNJ42829B ; 4) BURN PACK , Pack Number DYNJ54386C ; 5) LARGE BURN PACK , Pack Number DYNJ69770; 6) LARGE BURN PACK , Pack Number DYNJ69770A ; 7) SMALL BURN PACK , Pack Number DYNJ69797; 8) SMALL BURN PACK , Pack Number DYNJ69797A ; 9) BURN PACK-LF, Pack Number DYNJ82534; 10) BURN PACK-LF, Pack Number DYNJ82534H ; 11) BASIC BURN PACK , Pack Number DYNJ82729; 12) BURN PACK , Pack Number DYNJ83254; 13) BURN PACK , Pack Number DYNJ84744

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	DYNJ0781678S , Lot Number 19LMC634 ; DYNJ0781678S , Lot Number 20AMD173 ; DYNJ0781678S , Lot Number 20CMC665 ; DYNJ0… DYNJ0781678S , Lot Number 19LMC634 ; DYNJ0781678S , Lot Number 20AMD173 ; DYNJ0781678S , Lot Number 20CMC665 ; DYNJ0781678S , Lot Number 20EMB965 ; DYNJ0781678S , Lot Number 20GMC952 ; DYNJ0781678S , Lot Number 20JMD288 ; DYNJ0781678S , Lot Number 21CMB052 ; DYNJ0781678S , Lot Number 21CME303 ; DYNJ0781678S , Lot Number 21GME666 ; DYNJ0781678S , Lot Number 21IMD184 ; DYNJ0781678S , Lot Number 21KMG512 ; DYNJ0781678S , Lot Number 22AMF686 ; DYNJ0781678S , Lot Number 22BMA737 ; DYNJ0781678S , Lot Number 22DMI132 ; DYNJ0781678S , Lot Number 22EMB432 ; DYNJ0781678S , Lot Number 22EMI061 ; DYNJ0781678S , Lot Number 22GMB212 ; DYNJ0781678S , Lot Number 22IMC056 ; DYNJ0781678S , Lot Number 22KMB510 ; DYNJ0781678S , Lot Number 23AMD737 ; DYNJ0781678S , Lot Number 23BMC741 ; DYNJ0781678S , Lot Number 23CMG452 ; DYNJ0781678S , Lot Number 23EMJ106 ; DYNJ0781678S , Lot Number 23GMC393 ; DYNJ0781678S , Lot Number 23HMB925 ; DYNJ0781678S , Lot Number 23HMI837 ; DYNJ0781678S

code_info

DYNJ0781678S , Lot Number 19LMC634 ; DYNJ0781678S , Lot Number 20AMD173 ; DYNJ0781678S , Lot Number 20CMC665 ; DYNJ0…

DYNJ0781678S , Lot Number 19LMC634 ; DYNJ0781678S , Lot Number 20AMD173 ; DYNJ0781678S , Lot Number 20CMC665 ; DYNJ0781678S , Lot Number 20EMB965 ; DYNJ0781678S , Lot Number 20GMC952 ; DYNJ0781678S , Lot Number 20JMD288 ; DYNJ0781678S , Lot Number 21CMB052 ; DYNJ0781678S , Lot Number 21CME303 ; DYNJ0781678S , Lot Number 21GME666 ; DYNJ0781678S , Lot Number 21IMD184 ; DYNJ0781678S , Lot Number 21KMG512 ; DYNJ0781678S , Lot Number 22AMF686 ; DYNJ0781678S , Lot Number 22BMA737 ; DYNJ0781678S , Lot Number 22DMI132 ; DYNJ0781678S , Lot Number 22EMB432 ; DYNJ0781678S , Lot Number 22EMI061 ; DYNJ0781678S , Lot Number 22GMB212 ; DYNJ0781678S , Lot Number 22IMC056 ; DYNJ0781678S , Lot Number 22KMB510 ; DYNJ0781678S , Lot Number 23AMD737 ; DYNJ0781678S , Lot Number 23BMC741 ; DYNJ0781678S , Lot Number 23CMG452 ; DYNJ0781678S , Lot Number 23EMJ106 ; DYNJ0781678S , Lot Number 23GMC393 ; DYNJ0781678S , Lot Number 23HMB925 ; DYNJ0781678S , Lot Number 23HMI837 ; DYNJ0781678S

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-3061-2024%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.