CardioCommand recall
CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left…
Why was CardioCommand recalled?
Possible corrosion of the battery contact(s).
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?
Serial Numbers: 8059, 8060, 8022, 8063, 8211
- Product
- CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left…
- Recalling firm
- Cardiocommand Inc.
- Quantity
- 5 units
- Distribution
- US Nationwide distribution in the states of CT, VW, OH, IL, DE.
- Recall date
- June 19, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)