FDAClass IMay 24, 2023

ID Circuit Basic recall

ID Circuit Basic (P) 180, MP01340

Why was ID Circuit Basic recalled?

Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 04048675421870; All lots.

Product
ID Circuit Basic (P) 180, MP01340
Recalling firm
Draeger Medical, Inc.
Quantity
25 units
Distribution
Domestic: US Nationwide Distribution.
Recall date
May 24, 2023
Classification
Class I
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls