Arrow Epidural Catheterization KIT Ck-02220 recall
Arrow EPIDURAL CATHETERIZATION KIT CK-02220
Why was Arrow Epidural Catheterization KIT Ck-02220 recalled?
Product lidstock contains the incorrect expiration date for the product
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: 13F18A0713 13F18B0394
- Product
- Arrow EPIDURAL CATHETERIZATION KIT CK-02220
- Recalling firm
- Arrow International Inc
- Quantity
- 1360
- Distribution
- Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
- Recall date
- February 26, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)