Pneumothorax Kit recall
Pneumothorax Kit
Why was Pneumothorax Kit recalled?
Product packaging may not be completely sealed.
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?
AK 01500 CA 01500
- Product
- Pneumothorax Kit
- Recalling firm
- Arrow International Inc
- Quantity
- N/A
- Distribution
- Nationally
- Recall date
- April 11, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)