Medical device recalls Moderate risk

Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ90515…

Recall date
February 27, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1881-2026
FDA classification
Class II
Brand / firm
Medline Industries, LP
Sold / distributed
Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.

Why it was recalled

Unapproved design changes to the products outside of the 510(k) clearance.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ905153N GENERAL LAPAROSCOPY PACK DYNJ81602 LAPAROSCOPY DYNJ905157K, DYNJ905157L LAPAROTOMY PACK DYNJ46675G MAJOR LITHOTOMY PACK DYNJ81607 MAJOR PLUS PACK DYNJ905160O MINOR GENERAL PACK DYNJ81599

Get recall alerts

Free email alert whenever Medline Industries, LP has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Medline Industries, LP