Class II

Medical Device Recall: Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ905153N GENERAL LAPAROSCOPY PACK DYNJ81602 LAPAROSCOPY DYNJ905157K, DYNJ9

Medline Industries, LP · February 27, 2026

Reason for Recall

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

Product Description

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

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.

States Affected

NATIONWIDE

Quantity Affected

270,311 total

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1881-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.