---
title: "Smith’s Medical: CADD Infusion System Infusion Sets for use with CADD pumps — FDA announcement Jan 5, 2023 | Is It on Recall"
description: "Potential lack of delivery or underdelivery and false no disposable attached (NDA) alarms."
url: https://isitonrecall.com/recall/fdapress-fc03b32ff9458bc1-smith-s-medical-cadd-infusion-system-infusion-sets-for-use-with-cadd-pumps/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA company announcement

# Smith’s Medical: CADD Infusion System Infusion Sets for use with CADD pumps — FDA announcement Jan 5, 2023

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Jan 5, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: CADD Infusion System Infusion Sets for use with CADD pumps
- **Reason**: Potential lack of delivery or underdelivery and false no disposable attached (NDA) alarms.
- **Classification**: Not supplied
- **Recalling firm**: Smith’s Medical
- **Quantity**: Not supplied
- **Agency-reported status**: Company recall announcement
- **Source record identifier**: fc03b32ff9458bc1

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/smiths-medical-issues-urgent-medical-device-correction-letter-notifying-customers-potential-issues)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Smiths Medical Contact \| Contact Information \| Areas of Support; Global Complaint Management \| globalcomplaints@smiths-medical.com 1-(866)-216-8806 \| To report adverse events or product complaints; Technical Assistance \| 1-(800)-258-5361 \| Additional information or technical assistance |

Match all identifying details in the current notice. A brand name alone is not enough.

## Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

**FDA company announcement, table 1**

| Smiths Medical Contact | Contact Information | Areas of Support |
| --- | --- | --- |
| Global Complaint Management | globalcomplaints@smiths-medical.com 1-(866)-216-8806 | To report adverse events or product complaints |
| Technical Assistance | 1-(800)-258-5361 | Additional information or technical assistance |

Announcement retrieved Oct 1, 2026. [Official announcement](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/smiths-medical-issues-urgent-medical-device-correction-letter-notifying-customers-potential-issues).

## Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Fda listing date**: Jan 5, 2023
- **Company announcement date**: Dec 12, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

If you wish to contact the FDA regarding any adverse events or quality problems associated with this notice, use the following contact information.

[Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/smiths-medical-issues-urgent-medical-device-correction-letter-notifying-customers-potential-issues)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Smith’s Medical records](https://isitonrecall.com/brand/smith-s-medical/)