6F/7F MynxGrip Vascular Closure Device recall
6F/7F MynxGrip Vascular Closure Device; Product Model MX6721, Product Usage: The 6F/7F MynxGrip Vascular Closure Device is indicated for use to seal…
Why was 6F/7F MynxGrip Vascular Closure Device recalled?
A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.
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 No: F1609702, Expiry 4/20/2018; Lot No. F1534302, Expiry 12/31/2016
- Product
- 6F/7F MynxGrip Vascular Closure Device; Product Model MX6721, Product Usage: The 6F/7F MynxGrip Vascular Closure Device is indicated for use to seal…
- Recalling firm
- AccessClosure, Inc., A Cardinal Health Company
- Quantity
- 55 units
- Distribution
- US in the states of CA, and MS.
- Recall date
- August 10, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)