Reported Aug 14, 2024 · Ongoing
Medline procedure kits labeled as
MEDLINE INDUSTRIES, LP - Northfield
High riskUsing this product could cause serious injury, illness or death — stop using it now.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
11 of 11 products
| # | Product as published |
|---|---|
| 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 |
- Lot codes and dates
37 of 37 products
Products covered by this recall # Product as published 1 CMPJ08068F , Lot Number 24ABN950 2 CMPJ11455B , Lot Number 23IBD357 3 DYNJ26938J , Lot Number 22FBD709 4 DYNJ26938J , Lot Number 22GBH459 5 DYNJ26938J , Lot Number 22HBR225 6 DYNJ26938J , Lot Number 22IBJ562 7 DYNJ26938J , Lot Number 22JBP469 8 DYNJ26938J , Lot Number 23ABM365 9 DYNJ26938J , Lot Number 23CBM109 10 DYNJ26938J , Lot Number 23DBN340 11 DYNJ26938J , Lot Number 23GBH016 12 DYNJ26938J , Lot Number 23IBS867 13 DYNJ53018, Lot Number 21IBX266 14 DYNJ53018, Lot Number 22GBN555 15 DYNJ53018, Lot Number 23ABN207 16 DYNJ57729C , Lot Number 23HBK882 17 DYNJ57729C , Lot Number 24ABO025 18 DYNJ66856, Lot Number 21KBH003 19 DYNJ66856A , Lot Number 22DBD158 20 DYNJ66856A , Lot Number 22FBY433 - Amount recalled
- 1,679,067 units in total
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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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