Official recall record
Alaris™ Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite™ Y-site(s)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-05-03
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
BD has received customer reports of the Alaris™ Pump Infusion Set Low Sorbing Tubing (PE Lined) drip chamber becoming detached from the tubing. BD has confirmed that this issue is isolated to catalog number 10013072 only and a single batch (no. 22115368) where mis-assembly of the drip chamber to the tubing occurred. All other active catalog numbers containing a drip chamber are not affected. Recall start date: April 18, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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