RecallRadar

FDA Device recall Z-1453-2025

Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number 613034702

On 2025-04-02 the FDA classified a Class II recall of Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number 613034702 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 ma….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1453-2025
ClassificationClass II
Statusongoing
Initiated2025-02-11
Published2025-04-02
Last updated2026-09-13 11:57 UTC
CompanyMedline Industries Northfield
DistributionUS

Product

Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number 613034702

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) Pack Number 613034700: UDI/DI 10850009724004 (each) 40850009724005 (case), Lot Number 613034700; 2) Pack Number 61…1) Pack Number 613034700: UDI/DI 10850009724004 (each) 40850009724005 (case), Lot Number 613034700; 2) Pack Number 613034702: UDI/DI 10850009724066 (each) 40850009724067 (case), Lot Number 613034702

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-1453-2025%22

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