RecallRadar

FDA Device recall Z-0012-2025

CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24

On 2024-10-30 the FDA classified a Class II recall of CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24 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-0012-2025
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, YELLOW, Product Code 21-7300-24

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
UDI/DI 10610586027192, Lot Numbers: 3971732, 3971731, 4034016, 3977457, 4013365, 4019421, 4019422, 4034015, 4037744, 4…UDI/DI 10610586027192, Lot Numbers: 3971732, 3971731, 4034016, 3977457, 4013365, 4019421, 4019422, 4034015, 4037744, 4037745, 4034018, 4034017, 4046844, 4046843, 4053912, 4048899

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-0012-2025%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.