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
73 of 73 products
| # | Product as published |
|---|---|
| 1 | AV FISTULA PACK, Pack Number DYNJ80088 |
| 2 | AV FISTULA PACK-LF, Pack Number DYNJ0131782J |
| 3 | CABG, Pack Number DYNJ906462B |
| 4 | CABG ACCESSORY PACK-LF, Pack Number DYNJ0261346U |
| 5 | CARDIAC CATH PACEMAKER-LF, Pack Number DYNJ42997C |
| 6 | CARDIAC CATH PACK, Pack Number DYNJ61256A |
| 7 | CARDIAC CATH PACK-LF, Pack Number DYNJ61527 |
| 8 | CARDIAC CATH PACK-LF, Pack Number DYNJ53642C |
| 9 | CARDIOVASCULAR PACK LJ-LF, Pack Number DYNJ49635F |
| 10 | CAROTID PACK, Pack Number DYNJ0810062AI |
| 11 | CASTRO CABG-COMPONENT PACK, Pack Number DYNJ44857T |
| 12 | CATH PACK, Pack Number DYNJ59830A |
| 13 | CHOG CARDIAC CATH PACK, Pack Number SYNJ10304B |
| 14 | CICC, Pack Number DYNJ53854A |
| 15 | CMHP PACEMAKER PACK, Pack Number DYNJ30217G |
| 16 | DR NACKMAN VEIN PACK, Pack Number DYNJ56235 |
| 17 | ENDOVASCULAR AAA PACK-LF, Pack Number DYNJ55482F |
| 18 | EP DEVICE, Pack Number DYNJ65916B |
| 19 | EP STUDY PACK-LF, Pack Number DYNJ38059A |
| 20 | FHZ PACEMAKER PACK, Pack Number DYNJ36931D |
- Lot codes and dates
73 of 73 products
Products covered by this recall # Barcodes Product as published 1 1019532746754840195327467549Lot Number 23DBG477A; 2) Pack Number DYNJ0131782J: UDI/DI 10195327467548 (each) 40195327467549 (case) 2 1019532705788640195327057887Lot Number 23LMD975A; 3) Pack Number DYNJ906462B: UDI/DI 10195327057886 (each) 40195327057887 (case) 3 1019532705596740195327055968Lot Number 22GBV822Z; 4) Pack Number DYNJ0261346U: UDI/DI 10195327055967 (each) 40195327055968 (case) 4 1019348998842040193489988421Lot Number 22GMB113A; 5) Pack Number DYNJ42997C: UDI/DI 10193489988420 (each) 40193489988421 (case) 5 1019348969491840193489694919Lot Number 21JMG551A; 6) Pack Number DYNJ61256A: UDI/DI 10193489694918 (each) 40193489694919 (case) 6 1019348957888140193489578882Lot Number 23JBH403A; 7) Pack Number DYNJ61527: UDI/DI 10193489578881 (each) 40193489578882 (case) 7 1019348972160740193489721608Lot Number 21LBJ158A; 8) Pack Number DYNJ53642C: UDI/DI 10193489721607 (each) 40193489721608 (case) 8 1019532719140540195327191406Lot Number 24AMF039A; 9) Pack Number DYNJ49635F: UDI/DI 10195327191405 (each) 40195327191406 (case) 9 1019348986604940193489866040Lot Number 23LMF122A; 10) Pack Number DYNJ0810062AI: UDI/DI 10193489866049 (each) 40193489866040 (case) 10 1019532722195940195327221950Lot Number 22CMB582A; 11) Pack Number DYNJ44857T: UDI/DI 10195327221959 (each) 40195327221950 (case) 11 1019348957023640193489570237Lot Number 22JBD481Z; 12) Pack Number DYNJ59830A: UDI/DI 10193489570236 (each) 40193489570237 (case) 12 1019348978696540193489786966Lot Number 21EMF434A; 13) Pack Number SYNJ10304B: UDI/DI 10193489786965 (each) 40193489786966 (case) 13 1019348963151740193489631518Lot Number 21LBD584A; 14) Pack Number DYNJ53854A: UDI/DI 10193489631517 (each) 40193489631518 (case) 14 1019348992214140193489922142Lot Number 21GMB561A; 15) Pack Number DYNJ30217G: UDI/DI 10193489922141 (each) 40193489922142 (case) 15 1088994262155240889942621553Lot Number 23CBN679A; 16) Pack Number DYNJ56235: UDI/DI 10889942621552 (each) 40889942621553 (case) 16 1019532733227340195327332274Lot Number 23EBD843A; 17) Pack Number DYNJ55482F: UDI/DI 10195327332273 (each) 40195327332274 (case) 17 1019348990204440193489902045Lot Number 23BBS877A; 18) Pack Number DYNJ65916B: UDI/DI 10193489902044 (each) 40193489902045 (case) 18 1019348940111040193489401111Lot Number 23JBT190A; 19) Pack Number DYNJ38059A: UDI/DI 10193489401110 (each) 40193489401111 (case) 19 1019348992755940193489927550Lot Number 20LMF803A; 20) Pack Number DYNJ36931D: UDI/DI 10193489927559 (each) 40193489927550 (case) 20 1019348947563040193489475631Lot Number 23BBS364Z; 21) Pack Number DYNJ60618C: UDI/DI 10193489475630 (each) 40193489475631 (case) - Amount recalled
- 3860 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.
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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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