Microline Surgical ReNew Laproscopic Fenestrated recall
Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
Why was Microline Surgical ReNew Laproscopic Fenestrated recalled?
Potential for the Fenestrated Grasper Tip jaw to 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: 00115342
- Product
- Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
- Recalling firm
- Microline Surgical, Inc.
- Quantity
- 150 units
- Distribution
- Worldwide Distribution-USA including the states of CA, HI, ID, MA, MI, MS, PA, TN, UT, and TX. and the countries of Belgium, France, Ireland, Germany, Indonesia, Korea, Norway, Saudi Arabia, Switzerland, Turkey, and UK.
- Recall date
- July 9, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)