Reported Sep 18, 2024 · Ongoing
Medline Convenience 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 Convenience kits labeled as
10 of 10 products
| # | Product as published |
|---|---|
| 1 | KIT MANIFOLD CSTM-NORTHRIDGE, Pack Number 129736 |
| 2 | KIT LEFT HEART-VA MED, Pack Number 132701 |
| 3 | KIT MANIFOLD CSTM-RENAISSANC, Pack Number 134085 |
| 4 | KIT LEFT HEART- LEXINGTON , Pack Number 142643 |
| 5 | KIT ANGIO CSTM-SETON, Pack Number 143267 |
| 6 | SYR- VA HOSPITAL, Pack Number 144684 |
| 7 | BYPASS ENCOMPASS CDS, Pack Number CDS985003A |
| 8 | CSTM MANIFOLD KIT , Pack Number SAMPC0547 |
| 9 | CSTM MANIFOLD KIT - FRYE, Pack Number VASC1074 |
| 10 | CSTM MANIFOLD KIT , Pack Number VASC1130 |
- Lot codes and dates
67 of 67 products
Products covered by this recall # Product as published 1 Lot Number 20DKA054 ; 132701 2 Lot Number 24ADB481; 132701 3 Lot Number 24ADA120; 132701 4 Lot Number 23GDC081; 132701 5 Lot Number 23DDC268; 132701 6 Lot Number 23CDC677; 132701 7 Lot Number 22LDA569; 132701 8 Lot Number 22IDC180; 132701 9 Lot Number 22IDA238; 132701 10 Lot Number 22DDB501; 132701 11 Lot Number 22DDA530; 132701 12 Lot Number 22ADB638; 132701 13 Lot Number 21KDB209; 132701 14 Lot Number 21KDA233; 132701 15 Lot Number 21JDA611; 132701 16 Lot Number 21FDC090; 132701 17 Lot Number 21EDB524; 132701 18 Lot Number 21CDB488; 132701 19 Lot Number 20LDB085; 132701 20 Lot Number 20KDA727; 132701
This recall covers 106 products
The agency filed one notice per product. You are reading one of them; the other 105 are below.
93 more are in the archive.
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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