Baxter Electrocardiograph recall
Baxter Electrocardiograph, ELI 380 -DCS21
Why was Baxter Electrocardiograph recalled?
One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.
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?
Lot number 122420001706
- Product
- Baxter Electrocardiograph, ELI 380 -DCS21
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 1 unit
- Distribution
- TX
- Recall date
- February 1, 2023
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)