Recall
FDAHealthFebruary 25, 2026

Medline Industries, LP — Medline Kits: 1) D AND C PACK, Model Number: DYNJ41254B

⚠️ The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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) D AND C PACK, Model Number: DYNJ41254B
Lot code
25FBA224

Additional details

1) DYNJ41254B, UDI-DI: 10888277882003(each), 40888277882004(case), Lot Number: 25FBA224

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 12 units.

View original FDA notice →

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