RecallRadar

FDA Device recall Z-2625-2024

See RES Description

On 2024-09-04 the FDA classified a Class II recall of See RES Description 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

AgencyFDA Device
Recall numberZ-2625-2024
ClassificationClass II
Statusongoing
Initiated2024-04-08
Published2024-09-04
Last updated2026-09-13 11:57 UTC
CompanyMedline Industries Northfield
Distributionn/a

Product

See RES Description

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
DYNJ0708470K , Lot Number 19ALA269 ; DYNJ0708470K , Lot Number 19ELA237 ; DYNJ0708470K , Lot Number 19FLA396 ; DYNJ0…DYNJ0708470K , Lot Number 19ALA269 ; DYNJ0708470K , Lot Number 19ELA237 ; DYNJ0708470K , Lot Number 19FLA396 ; DYNJ0708470K , Lot Number 19GLA166 ; DYNJ0708470K , Lot Number 19HLA649 ; DYNJ0708470K , Lot Number 19ILA054 ; DYNJ0708470K , Lot Number 19JLA505 ; DYNJ0708470K , Lot Number 19KLA167 ; DYNJ0708470K , Lot Number 19LLA455 ; DYNJ0844004, Lot Number 19AKB795 ; DYNJ0844004, Lot Number 19DKC239 ; DYNJ0844004, Lot Number 19EKB799 ; DYNJ0844004, Lot Number 19FKB763 ; DYNJ0844004, Lot Number 19GKB309 ; DYNJ0844004, Lot Number 19HKC027 ; DYNJ0844004, Lot Number 19IKB582 ; DYNJ0844004, Lot Number 19JKB630 ; DYNJ0844004, Lot Number 19KKB713 ; DYNJ0934752F , Lot Number 20LLA127 ; DYNJ0934752F , Lot Number 21ALA602 ; DYNJ0934752F , Lot Number 21DLA714 ; DYNJ0934752F , Lot Number 21FLA405 ; DYNJ0934752F , Lot Number 21GLB256 ; DYNJ0934752F , Lot Number 21ILA246 ; DYNJ0934752F , Lot Number 21KLA976 ; DYNJ0934752F , Lot Number 22ALA019 ; DYNJ0934752F , Lot Number 22CL

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-2625-2024%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.