Data Foundry

Medical device recalls 2020

Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32 — Class II medical device recall Z-2959-2020

Terminated recall by Terumo Cardiovascular Systems Corporation, reported 2020-09-23, distributed nationwide. Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) se

Recall numberZ-2959-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTerumo Cardiovascular Systems Corporation, Ann Arbor, MI, United States
Recall initiated2020-08-25
Classified2020-09-11
Reported by FDA2020-09-23
Terminated2021-01-29
DistributedNationwide (US)
Quantity100
UPC / GTIN / UDI-DI00886799000038
Serial numbers20288, 20289, 20290, 20291, 20292, 20293, 20294, 20295, 20296, 20299, 20300, 20301, 20302, 20306, 20307, 20308, 20309, 20310, 20312, 20317, 20318, 20320, 20321, 20322, 20323 and 75 more
Model numbers5773

Product

Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32, Catalog Number 5773 - Product Usage: intended for use with Terumo and Sarns brand air detection and heart-lung systems to detect gross air bubbles in the line during extracorporeal procedures.

Reason for recall

Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the mating wire connector. This intermittent connection may result in false air bubble alarms.

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-2959-2020. 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.