Recall
FDAHealthFebruary 25, 2026

Medline Industries, LP — Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257F

⚠️ The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
February 25, 2026

US Nationwide distribution.

What's affected?

Product
Medline Kits: 1) GYN LAPAROSCOPY PACK, Model Number: DYNJ41257F
Lot code
25GBL423

Additional details

1) DYNJ41257F, UDI-DI: 10193489708523(each), 40193489708524(case), Lot Number: 25GBL423

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 6 units.

View original FDA notice →

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