Recall
FDAHealthFebruary 25, 2026

Medline Industries, LP — Medline Kits: 1) HYSTEROSCOPY PACK, Model Number: DYNJ48399C; 2) SLING PACK, Model Number: DYNJ62849B

⚠️ The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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) HYSTEROSCOPY PACK, Model Number: DYNJ48399C; 2) SLING PACK, Model Number: DYNJ62849B
Lot code
24CBU779

Additional details

1) DYNJ48399C, UDI-DI: 10195327172626(each), 40195327172627(case), Lot Number: 24CBU779; 2) DYNJ62849B, UDI-DI: 10195327514884(each), 40195327514885(case), Lot Number: 24BBS275

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 89 units.

View original FDA notice →

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