Z-2444-2024 Class I Ongoing
FDA device recall Z-2444-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Apr 8, 2024 and is designated Class I. 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. Affected quantity: 1,679,067 units in total.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 14, 2024
- Initiation Date
- Apr 8, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,679,067 units in total
Product Description
Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ; 4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ; 5) ARTERIOGRAM PACK, Pack Number DYNJ53018; 6) CATH PACK , Pack Number DYNJ57729C ; 7) PEDS CATH PACK, Pack Number DYNJ66856; 8) PEDS CATH PACK, Pack Number DYNJ66856A ; 9) STEWARD ROCKLEDGE CATH RRS, Pack Number DYNJ81061A ; 10) CATH LAB PACK , Pack Number DYNJ84617; 11) UA/UV CATHETERIZATION TRAY, Pack Number UVT1190A
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 Distribution: US (nationwide) and OUS countries of: AE, AI, BB, CA, CL, CY, DE, GT, HN, JP, MX, MY, PA, PE, PR, SA, SG, TC, TT, VI, PR, TT, MX, BM, ES, NI, DO, GU, CR, AT, CD, DE, DF, W, and ON.
Code Information
CMPJ08068F , Lot Number 24ABN950 ; CMPJ11455B , Lot Number 23IBD357 ; DYNJ26938J , Lot Number 22FBD709 ; DYNJ26938J , Lot Number 22GBH459 ; DYNJ26938J , Lot Number 22HBR225 ; DYNJ26938J , Lot Number 22IBJ562 ; DYNJ26938J , Lot Number 22JBP469 ; DYNJ26938J , Lot Number 23ABM365 ; DYNJ26938J , Lot Number 23CBM109 ; DYNJ26938J , Lot Number 23DBN340 ; DYNJ26938J , Lot Number 23GBH016 ; DYNJ26938J , Lot Number 23IBS867 ; DYNJ53018, Lot Number 21IBX266 ; DYNJ53018, Lot Number 22GBN555 ; DYNJ53018, Lot Number 23ABN207 ; DYNJ57729C , Lot Number 23HBK882 ; DYNJ57729C , Lot Number 24ABO025 ; DYNJ66856, Lot Number 21KBH003 ; DYNJ66856A , Lot Number 22DBD158 ; DYNJ66856A , Lot Number 22FBY433 ; DYNJ66856A , Lot Number 22GBK576 ; DYNJ66856A , Lot Number 22HBQ139 ; DYNJ66856A , Lot Number 22IBO303 ; DYNJ66856A , Lot Number 22JBO861 ; DYNJ66856A , Lot Number 22JBQ914 ; DYNJ66856A , Lot Number 23ABT952 ; DYNJ66856A , Lot Number 23CBF157 ; DYNJ66856A , Lot Number 23EBE461 ; DYNJ66856A , Lot Number 23EBI477 ; DYNJ66856A , Lot Number 23HBD973 ; DYNJ81061A , Lot Number 23HBN396 ; DYNJ84617, Lot Number 23FBR368 ; DYNJ49920L , Lot Number 23KMB066 ; UVT1190A , Lot Number 23BLA187 ; UVT1190A , Lot Number 23DLA246 ; UVT1190A , Lot Number 23KLA117 ; UVT1190A , Lot Number 23LLA329
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2444-2024
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026