RecallRadar

FDA Device recall Z-2746-2024

Medline procedural kits labeled as: 1) BIOPSY PACK, Pack Number DYNJ63370A

On 2024-09-04 the FDA classified a Class II recall of Medline procedural kits labeled as: 1) BIOPSY PACK, Pack Number DYNJ63370A 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-2746-2024
ClassificationClass II
Statusongoing
Initiated2024-04-08
Published2024-09-04
Last updated2026-09-13 11:57 UTC
CompanyMedline Industries Northfield
Distributionn/a

Product

Medline procedural kits labeled as: 1) BIOPSY PACK, Pack Number DYNJ63370A; 2) CIRCUMCISION TRAY, Pack Number CIT7210; 3) CIRCUMCISION TRAY, Pack Number DYNDA2271; 4) MERCY MEDICAL CIRCUMCISION TRAY, Pack Number CIT6780; 5) UCLA - BREAST BIOPSY KITDYNDH1512A

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
1) DYNJ63370A , Lot Number 23IMB164 ; 2) CIT7210, Lot Number 2022101890; 3) DYNDA2271, Lot Number 2023090790; 4) CIT…1) DYNJ63370A , Lot Number 23IMB164 ; 2) CIT7210, Lot Number 2022101890; 3) DYNDA2271, Lot Number 2023090790; 4) CIT6780, Lot Number 2022101890; 5) DYNDH1512A, Lot Number 2023090790

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-2746-2024%22

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