RecallRadar

FDA Device recall Z-0015-2025

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

On 2024-10-30 the FDA classified a Class II recall of CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24JP by Smiths Medical Asd, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0015-2025
ClassificationClass II
Statusongoing
Initiated2024-06-26
Published2024-10-30
Last updated2026-09-13 11:57 UTC
CompanySmiths Medical Asd
Distributionn/a

Product

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

Reason

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.

Identifiers

code_info
UID/DI NA, Lot/Serial Numbers: 3983315, 3971709, 3983316, 3983320, 3983329, 4013361, 4013363, 4013373, 4013377, 40133…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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0015-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.