Angiodynamics 5F Standard Micro-Introducer Kit recall
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog…
Why was Angiodynamics 5F Standard Micro-Introducer Kit recalled?
5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component
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: 5626935 Expiration Date: 08/31/2023
- Product
- Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog…
- Recalling firm
- Angiodynamics, Inc.
- Quantity
- 32 kits
- Distribution
- US Nationwide distribution including in the states of AL, CT, GA, FL.
- Recall date
- November 11, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)