B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number correcte... — FDA record Z-0265-2023

Reported terminated

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 Sep 15, 2022. 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
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
Reason
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Classification
Class II
Recalling firm
Medical Action Industries, Inc. 306
Quantity
240 cases of 20 units
Agency-reported status
Terminated
Source record identifier
Z-0265-2023

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 applicabilityUDI/DI 10809160283875, Batch/Lot number 298442

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

Distribution

US Nationwide distribution in the state of Pennsylvania.

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
Nov 30, 2022
Recall initiation date
Sep 15, 2022
Center classification date
Nov 18, 2022
Termination date
Feb 19, 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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