Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included. 50mL, Product Code 21-7001-24
FDA Recall Z-2522-2025 · Posted 2025-09-04
Recalling FirmICU Medical Inc.
Recall StatusOpen, Classified
Product CodeFPA
Date Initiated2025-08-06
Product Quantity29811 units
Reason for Recall
Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
Firm Action
ICU Medical issued an URGENT: MEDICAL DEVICE CORRECTION notice to its consignees on 08/06/2025 via registered mail and email. The notice explained the issue, potential risk can requested the following:
Customer Required Actions:
Please complete the following actions below.
1. Review your inventory of CADD Medication Cassette Reservoirs to confirm if any of the affected lots are within your possession.
2. Quarantine the affected product and destroy or discard it immediately following your institution s process for destruction or discarding.
3. Return the attached Customer Response Form to [email protected] within ten (10) days of receipt to acknowledge your understanding of this notification.
4. DISTRIBUTORS: Immediately forward this notice to all users to whom you distributed these products. Request that they complete the Customer Response Form and return it to [email protected].
For further inquires:
- To report adverse events or product complaints: Global Complaint Management: [email protected]; 1-(866)-216-8806
- Additional information or to request replacement product: Customer Service:
[email protected]; 1-(800)-258-5361
- Questions about this communication: Field Action Processing: [email protected]; 1-(844)-861-6220
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.