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U.S. Department of Health and Human Services

Class 2 Device Recall 18 gauge thin wall needle

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 Class 2 Device Recall 18 gauge thin wall needlesee related information
Date Initiated by FirmDecember 17, 2003
Date PostedFebruary 24, 2004
Recall Status1 Terminated 3 on July 27, 2004
Recall NumberZ-0543-04
Recall Event ID 28167
510(K)NumberK961552 
Product Classification Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days - Product Code FOZ
Product18 Gauge thin wall needle as part of a Central Venous Catheter Kit
Code Information List No. 414000413, Lot No. 02053SN, 02062SN, 03307SN, 04064SN, 05248SN, 05308SN, 06248SN, 93297SN, 96294SN. List No. 414000415, Lot No. 04240SN, 04241SN. List No. 414010423, Lot No. 02057SN, 02065SN, 03257SN, 04238SN, 05341SN, 06249SN, 93208SN, 94194SN, 95224SN, 96054SN. List No. 414010425, Lot No. 02051SN, 02058SN. List No. 414050415, Lot No. 04239SN, 06244SN, 07244SN, 95221SN. List No. 414060423, Lot No. 02059SN, 03261SN, 06245SN, 93206SN, 95220SN, 95232SN. List No. 414070423, Lot No. 02354SN, 03258SN, 95222SN. List No. 414110423, Lot No. 02052SN, 03259SN, 05342SN, 07250SN, 93296SN, 94196SN, 95233SN. List No. 414110425, Lot No. 02049SAN, 03260SAN, 93207SN. List No. 414130415, Lot No. 02050SN, 04065SN, 05249SN, 95223SN, 95229SN. List No. 414140423, Lot No. 02061SN, 04063SN, 06247SN, 94195SN, 95231SN, 96056SN. 
FEI Number 1415939
Recalling Firm/
Manufacturer		 Abbott Laboratories HPD/ADD/GPRD
100/200 Abbott Park Road
Abbott Park IL 60064
For Additional Information Contact
847-937-4525
Manufacturer Reason
for Recall		18 gauge needles in Central Venous Catheter kits may be partially occluded.
FDA Determined
Cause 2		Other
ActionConsignees were notified by FedEx letter on 12/17/2003.
Quantity in Commerce93564
DistributionNationwide including VA facilities in ID and NC. Foreign distribution to Australia, Austria, Belgium, Brazil, Canada, Chile, Columbia, Dominican Republic, Egypt, Greece, Ireland, Italy, Japan, Malaysia, Portugal, Slovenia, Spain, Switzerland, Turkey, UK, United Arab Emirates.
Total Product Life CycleTPLC Device Report
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.
510(K) Database510(K)s with Product Code = FOZ
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