FDAFDA · Food and drugs·Recall number Z-0465-2014
Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue.
Published December 18, 2013 · Recall initiated: November 6, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the 33821WTD Wavy grasper was mislabeled as 33821DYD Axillent Debakey Grasping Forceps.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Karl Storz Endoscopy America Inc
- Distributor
- Nationwide Distribution including states of: TX, PA, and NY.
- Lot
- Lot Code YX
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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