Reported Aug 28, 2024 · Ongoing
Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYK1012268E1
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 medical
- procedure kits labeled as followsa) ENDO KIT, REF DYK1012268E1
- Lot codes and dates
a) REF DYK1012268E1UDI/DI 40884389919089 (case)10884389919088 (unit)
- Lot Numbers
22FBU93122HBL61922JBG19222LBH95723CBU46723FBS31923IBT78923KMH977
- Amount recalled
- 2588 units
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
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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