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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:182568

CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous, intra-arterial, epidural, in close proximity to nerves, and into an intra-operative site (soft tissue/body cavity/surgical wound site).

Official recall number

Z-0529-2021

Evidence summary

Product code
FRN
Recall status
Terminated
Event initiated
July 30, 2020
Root cause
Other
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0529-2021

Field note

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