FDAClass IINovember 30, 2022

B. Braun CARESITE Port Access Kit w/Tegaderm recall

B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)

Why was B. Braun CARESITE Port Access Kit w/Tegaderm recalled?

The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 10809160283875, Batch/Lot number 298442

Product
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
Recalling firm
Medical Action Industries, Inc. 306
Quantity
240 cases of 20 units
Distribution
US Nationwide distribution in the state of Pennsylvania.
Recall date
November 30, 2022
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls