FDAClass IIOctober 30, 2024

CADD Medication Cassette Reservoir recall

CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24JP

Why was CADD Medication Cassette Reservoir recalled?

Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

UID/DI NA, Lot/Serial Numbers: 3983315, 3971709, 3983316, 3983320, 3983329, 4013361, 4013363, 4013373, 4013377, 4013378, 4019427, 4019429, 4034028, 4037753, 4052410, 4040250, 4042843, 4048894, 4046846, 4052412, 4052413

Product
CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24JP
Recalling firm
Smiths Medical ASD Inc.
Quantity
109563 units
Distribution
Worldwide distribution.
Recall date
October 30, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls