Reported Nov 15, 2023 · Ongoing
BD Alaris Syringe Module, REF 8110
CareFusion 303, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
- BD Alaris Syringe Module, REF 8110
- Lot codes and dates
- All Lots/ UDI-DI
10885403516047108854035153231088540381104310885403515255 1088540381103610885403515262108854038110121088540351527910885403424267
- All Lots/ UDI-DI
- Amount recalled
- 133,727 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Stop using this product now
Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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