Reported May 28, 2014 · Terminated
Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasper…
Microline Surgical
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Microline Surgical · 50 Dunham Rd · Beverly, MA · 01915-1882
Is this the product you have?
- Microline Renew Fenestrated Control Tip Grasper, Single Patient Use
- Product Number3222 The ReNew Fenestrated Grasper Forceps Tips are intended to cut, grasp, and dissect various abdominal tissue for use in endoscopic, including laproscopic surgical procedures where instruments are introduced onto the body through a cannula
- Lot codes and dates
- Lot Numbers00116169 and 00115866
- Amount recalled
- 540 units
Where it was sold
Why it was recalled
Grasper jaw may break when force is applied to the jaw
This product could cause temporary or reversible health problems — stop using it.
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