Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH ... — FDA record Z-2419-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 27, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C
Reason
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Classification
Class II
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total
Agency-reported status
Ongoing
Source record identifier
Z-2419-2026

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityDYNDC3525 UDI-DI 10198459576294 Lot 25KBM985 DT13191A UDI-DI 10653160998914 Lot 26AMA168 CDS982047S UDI-DI 10198459385735 Lot 26AMB202 DYNJ62889C UDI-DI 10198459416453 Lot 26AMA584

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution. OUS distribution pending.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jun 24, 2026
Recall initiation date
Apr 27, 2026
Center classification date
Jun 12, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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