MEDLINE INDUSTRIES, LP - Northfield 2024-11-20 Health serious FDA
Health · FDA · Recall #FDA-Z-0355-2025
Lab Kit, SKU DYLAB1018; Component No. 503581 Recall
Issued November 20, 2024 · MEDLINE INDUSTRIES, LP - Northfield
In November 2024, MEDLINE INDUSTRIES, LP - Northfield recalled the Lab Kit, SKU DYLAB1018; Component No. 503581, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged hospitalization.
What you should do
- 1 Stop using Lab Kit, SKU DYLAB1018; Component No. 503581 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MEDLINE INDUSTRIES, LP - Northfield to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- November 20, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AL, CA, FL, GA, IL, KY, MO, MS, MT, TN, TX, VA and WA.
- Recall number
- FDA-Z-0355-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- MEDLINE INDUSTRIES, LP - Northfield has 108 recalls in our database, including 12 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.