Syringe Pumps_bd Swissco
- Recalling firm
- Becton Dickinson Ltd
- Product
- Syringe Pumps_BD SwissCo. [Device]. Model: BD Alaris™ neXus and Alaris™ Plus syringe pumps. Affected: Catalog number - 8002TIG03, 8002TIG03-G, 8003TIG03, 8003TIG03-G, 8005TIG03, CCneXus1, CCneXus1-S, PKneXus1 - All serial numbers
- Reason
- The manufacturer has identified through an internal investigation that the BD Alaris™ neXus and Alaris™ Plus syringe pumps may develop a mechanical anomaly on the linear potentiometer if the device is not stored in the correct position. The syringe plunger moves along the linear potentiometer component during infusion., This is an internal component and not readily visible to the Clinical User. If this anomaly occurs, it can lead to incorrect sensor readings, which may trigger error codes PL3, PL8, or PL9., These PL error codes are an intentional design feature that notify the Clinical...
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-03-12
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/3c9852a2-9662-44a3-88ca-db1a2969db94