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U.S. Department of Health and Human Services

Class 2 Device Recall AccuSure

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  Class 2 Device Recall AccuSure see related information
Date Initiated by Firm April 09, 2009
Date Posted June 24, 2009
Recall Status1 Terminated 3 on November 01, 2010
Recall Number Z-1504-2009
Recall Event ID 51817
510(K)Number K070917  
Product Classification insulin syringe - Product Code FMF
Product AccuSure, U-100 31 Gauge, 1cc Insulin Syringe, 5/16" (8mm) Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-7002-2
Code Information Lot A07001, exp 07/2012
Recalling Firm/
Manufacturer		 Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
120 Vintage Dr Ne
Huntsville AL 35811-8216
For Additional Information Contact Mr. Larry Kass
256-859-2222
Manufacturer Reason
for Recall		 Needles separate from the barrel of the syringes.
FDA Determined
Cause 2		 Nonconforming Material/Component
Action On 04/09/2009, Qualitest issued a press release and sent out recall notifications to their consignees by US Mail. The recall was extended to the User level. Qualitest will send a second letter to all non-responders after thirty days. Thirty days after the second letter, Qualitest will perform a recall effectiveness check by telephone on a percentage of non-responders (in accordance with FDA request).
Quantity in Commerce 559,500 syringes
Distribution Nationwide.
Total Product Life Cycle TPLC 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) Database 510(K)s with Product Code = FMF and Original Applicant = FEEL TECH
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