Microline Renew Fenestrated Control Tip Grasper recall
Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasper Forceps Tips are intended to…
Why was Microline Renew Fenestrated Control Tip Grasper recalled?
Grasper jaw may break when force is applied to the jaw
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 Numbers: 00116169 and 00115866
- Product
- Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasper Forceps Tips are intended to…
- Recalling firm
- Microline Surgical
- Quantity
- 540 units
- Distribution
- Worldwide Distribution - US including the states of TX, IL, TN and NY, and the country of Chile.
- Recall date
- May 28, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)