Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098 — FDA record Z-1393-2025

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 Feb 11, 2025. 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 procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098
Reason
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Classification
Class II
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Quantity
456 kits
Agency-reported status
Ongoing
Source record identifier
Z-1393-2025

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 applicability1) 10195327273132 (each) 40195327273133 (case), Lot Number 23GBK039Z

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

Distribution

Worldwide - US Nationwide and the country of Canada.

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
Mar 26, 2025
Recall initiation date
Feb 11, 2025
Center classification date
Mar 18, 2025

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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