Z-2739-2024 Class II Ongoing
FDA device recall Z-2739-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Apr 8, 2024 and is designated Class II. Reason for recall: 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… The recall status is ongoing.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 4, 2024
- Initiation Date
- Apr 8, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
Medline procedural kits labeled as: 1) ANESTHESIA CIRCUIT PEDS-LF, Pack Number DYNJAA0327F; 2) ANESTHESIA CIRCUIT PEDS-LF, Pack Number DYNJAA0327G
Reason for Recall
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.
Distribution Pattern
Worldwide
Code Information
DYNJAA0327F , Lot Number 20LBV329 ; DYNJAA0327G , Lot Number 21FBM358 ; DYNJAA0327G , Lot Number 22CBY412 ; DYNJAA0327G , Lot Number 22GBZ157 ; DYNJAA0327G , Lot Number 22JBR268 ; DYNJAA0327G , Lot Number 23BBL309 ; DYNJAA0327G , Lot Number 23HBU238 ; DYNJAA0327G , Lot Number 23KBB605 ; DYNJAA0327G , Lot Number 24CBJ211 ;
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2739-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026