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U.S. Department of Health and Human Services

Class 2 Device Recall CIDEX OPA

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 Class 2 Device Recall CIDEX OPAsee related information
Date Initiated by FirmJune 01, 2012
Date PostedAugust 27, 2012
Recall Status1 Terminated 3 on September 11, 2013
Recall NumberZ-2276-2012
Recall Event ID 62919
510(K)NumberK030004 
Product Classification Sterilant, medical devices - Product Code MED
ProductCIDEX OPA, High Level Disinfectant Solution, Glutaraldehyde-free (0.55% ortho-phthaladehyde) solution. The CIDEX OPA solution is intended for automated and manual cleaning and disinfection.
Code Information Product codes: 20390 (US).
FEI Number 3003662624
Recalling Firm/
Manufacturer		 Advanced Sterilization Products
33 Technology Dr
Irvine CA 92618-2346
For Additional Information Contact
949-453-6400
Manufacturer Reason
for Recall		The recall was initiated because Advanced Sterilization Products has discovered instances of missing labels on bottles of CIDEX OPA Solution, Part # 20390 manufactured between May 2011 and April 2012.
FDA Determined
Cause 2		Process control
ActionAn "Urgent Medical Device Recall" letter dated August 10, 2012 was sent to all customers who purchased the CIDEX OPA solution, part #20390 (manufactured between May 2011 and April 2012). The letter informed the customers of the problem identified and the actions to be taken. Customers were instructed to notify their customers if they have distributed bottles of CIDEX OPA Solution to other locations. Customers were instructed to call Stericycle at (866) 629-6182 to arrange for return of the product.
Quantity in Commerce1,310,844 units
DistributionNationwide (USA) and Puerto Rico.
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 = MED
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