Reported Apr 2, 2025 · Ongoing
Medline procedure kits labeled as
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline procedure kits labeled as
34 of 34 products
| # | Product as published |
|---|---|
| 1 | ANGIO DRAPE PACK (DRLUL)-LF, Pack Number DYNJ47718D |
| 2 | ANGIO PACK, Pack Number DYNJ69678 |
| 3 | ANGIOGRAPHY CV RAD PACK, Pack Number DYNJ64936A |
| 4 | ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ49621C |
| 5 | ANGIOGRAPHY PACK, Pack Number DYNJ61266A |
| 6 | ANGIOGRAPHY PACK-LF, Pack Number DYNJ35916N |
| 7 | ARTERIOGRAM PACK, Pack Number DYNJ34442F |
| 8 | CARDIAC CATH FEMORAL PACK, Pack Number DYNJ53588I |
| 9 | CARDIAC CATH PACK, Pack Number DYNJ31733C |
| 10 | CARDIAC CATH PACK, Pack Number DYNJ41315A |
| 11 | CARDIAC CATH PACK-LF, Pack Number DYNJ0380198L |
| 12 | CATH LAB PACK, Pack Number 0M-CP31796Q |
| 13 | CATH LAB PACK-LF, Pack Number DYNJ0194968AG |
| 14 | CATH LAB TRAY, Pack Number 00-401610J |
| 15 | CHRISTUS SR CATH LAB PACK, Pack Number DYNJ60931C |
| 16 | CRMC CATH LAB TRAY JUDKINS-LF, Pack Number DYNJ61088F |
| 17 | CRMC NEURO ENDO HYBRID-LF, Pack Number DYNJ61101D |
| 18 | EP PACK MORNINGSIDE, Pack Number DYNJ69301 |
| 19 | FEMORAL TRAY 2, Pack Number DYNJ68812C |
| 20 | INTERVENTIONAL MINOR PACK, Pack Number DYNJ24615D |
- Lot codes and dates
34 of 34 products
Products covered by this recall # Barcodes Product as published 1 1019348996815640193489968157Lot Number 23LME887A; 2) Pack Number DYNJ69678: UDI/DI 10193489968156 (each) 40193489968157 (case) 2 1019348997875940193489978750Lot Number 23EMD520A; 3) Pack Number DYNJ64936A: UDI/DI 10193489978759 (each) 40193489978750 (case) 3 1019532700858140195327008582Lot Number 21LBW389A; 4) Pack Number DYNJ49621C: UDI/DI 10195327008581 (each) 40195327008582 (case) 4 1019532705776340195327057764Lot Number 23LMG954A; 5) Pack Number DYNJ61266A: UDI/DI 10195327057763 (each) 40195327057764 (case) 5 1019532722397740195327223978Lot Number 23GBF536A; 6) Pack Number DYNJ35916N: UDI/DI 10195327223977 (each) 40195327223978 (case) 6 1019348988142440193489881425Lot Number 23EBE626A; 7) Pack Number DYNJ34442F: UDI/DI 10193489881424 (each) 40193489881425 (case) 7 1019532701400140195327014002Lot Number 23LMG342A; 8) Pack Number DYNJ53588I: UDI/DI 10195327014001 (each) 40195327014002 (case) 8 1088994287529040889942875291Lot Number 23EME005A; 9) Pack Number DYNJ31733C: UDI/DI 10889942875290 (each) 40889942875291 (case) 9 1088827790708940888277907080Lot Number 21BBG459B; 10) Pack Number DYNJ41315A: UDI/DI 10888277907089 (each) 40888277907080 (case) 10 1019348991647840193489916479Lot Number 22LBA182A; 11) Pack Number DYNJ0380198L: UDI/DI 10193489916478 (each) 40193489916479 (case) 11 1088994275648340889942756484Lot Number 22GBH915A; 12) Pack Number 0M-CP31796Q: UDI/DI 10889942756483 (each) 40889942756484 (case) 12 1019532717955740195327179558Lot Number 21HBP168A; 13) Pack Number DYNJ0194968AG: UDI/DI 10195327179557 (each) 40195327179558 (case) 13 1088994273164040889942731641Lot Number 24AME980A; 14) Pack Number 00-401610J: UDI/DI 10889942731640 (each) 40889942731641 (case) 14 1019348995294040193489952941Lot Number 23LBL085Z; 15) Pack Number DYNJ60931C: UDI/DI 10193489952940 (each) 40193489952941 (case) 15 1019532745158540195327451586Lot Number 21JMI207A; 16) Pack Number DYNJ61088F: UDI/DI 10195327451585 (each) 40195327451586 (case) 16 1019532745181340195327451814Lot Number 23LMG703A; 17) Pack Number DYNJ61101D: UDI/DI 10195327451813 (each) 40195327451814 (case) 17 1019348992610140193489926102Lot Number 23HME348A; 18) Pack Number DYNJ69301: UDI/DI 10193489926101 (each) 40193489926102 (case) 18 1019532744945240195327449453Lot Number 23CBL353A; 19) Pack Number DYNJ68812C: UDI/DI 10195327449452 (each) 40195327449453 (case) 19 1088994243605740889942436058Lot Number 23KMC169A; 20) Pack Number DYNJ24615D: UDI/DI 10889942436057 (each) 40889942436058 (case) 20 1088994247450940889942474500Lot Number 21JMF491A; 21) Pack Number DYNJ54253: UDI/DI 10889942474509 (each) 40889942474500 (case) - Amount recalled
- 9246 units
This recall covers 29 products
The agency filed one notice per product. You are reading one of them; the other 28 are below.
16 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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