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Class 2 Device Recall AR1000 Qoustic Qurette" |
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Date Initiated by Firm |
November 05, 2012 |
Date Posted |
December 17, 2012 |
Recall Status1 |
Terminated 3 on March 04, 2015 |
Recall Number |
Z-0534-2013 |
Recall Event ID |
63808 |
510(K)Number |
K062544
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Product Classification |
Instrument, ultrasonic surgical - Product Code LFL
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Product |
Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Wound Therapy System.
Major components of the AR1000 Wound Therapy System include an ultrasonic generator, converter hand piece, done-shaped applicator tip (qurette), and a saline supply reservoir.
Product Usage: The Arobella Medical AR1000 Wound Therapy System is interned for the selective dissection and fragmentation of tissue, wound debridement ( of acute and chronic wounds, burns, and diseased or necrotic tissue), and cleansing irrigation of the wound site for the removal of debris, exudates, fragments, and other matter.
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Code Information |
0001 and 0002 |
Recalling Firm/ Manufacturer |
Arobella Medical, LLC 5929 Baker Rd Ste 470 Minnetonka MN 55345-4770
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For Additional Information Contact |
952-345-6840
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Manufacturer Reason for Recall |
This recall has been initiated because the Arobella Medical 6mm Qurette Q07 Lot Numbers 0001 and 0002 can fracture during use and may release a fragment or fragments. The 6 mm Qurette is a component of the AR1000 Quostic Wound Therapy System.
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FDA Determined Cause 2 |
Nonconforming Material/Component |
Action |
Arobella Medical sent an " Urgent: Medical Device Recall" letter dated November 2, 2012 to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to immediately examine their inventory, quarantine and return any product subject to the recall. If the affected product have been further distributed, customers were advised to notify their customers of the product recall. For questions call 952-288-2810. |
Quantity in Commerce |
99 |
Distribution |
Worldwide distribution - US (nationwide) and the states of AL, CA, ID, IN, IA, MI, MN, MS, NJ, NM, OH, PA. SC, TX, UT, VA, WI. including the country of SAUDI ARABIA. |
Total Product Life Cycle |
TPLC Device Report
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database |
510(K)s with Product Code = LFL and Original Applicant = AROBELLA MEDICAL, LLC
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