Recall
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BASIC CL PACK-LF DYNJ87052 BASIC PACK DYNJ83976 BASIC SET UP…
Medline Industries, LP · 27 Feb 2026
- Status
- Recall open, classified
- Why, in the FDA's words
- “Unapproved design changes to the products outside of the 510(k) clearance.”
- Recall began
- 27 Feb 2026
- Company
- Medline Industries, LP
- Device type
- Product code (LRO)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.