Launcher Guiding Catheter recall
Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
Why was Launcher Guiding Catheter recalled?
Device packaging may not be 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?
Lot #481938U
- Product
- Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
- Recalling firm
- Stryker Sustainability Solutions
- Quantity
- 2
- Distribution
- US distribution to KY.
- Recall date
- May 18, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)