Alaris Pump Infusion Set Low Sorbing Tubing — Class II medical device recall Z-1944-2024
Ongoing recall by BD SWITZERLAND SARL, reported 2024-06-12, distributed nationwide. Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatm
| Recall number | Z-1944-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | BD SWITZERLAND SARL, Eysins, N/A, Switzerland |
| Recall initiated | 2024-04-18 |
| Classified | 2024-05-31 |
| Reported by FDA | 2024-06-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 11.3 sets |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 07613203021210 |
| Lot numbers | 22115368 |
| Model numbers | 10013072 |
Product
Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products.
Reason for recall
Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1944-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.