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U.S. Department of Health and Human Services

Class 2 Device Recall Alinity i Total BetahCG Reagent Kit

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 Class 2 Device Recall Alinity i Total BetahCG Reagent Kitsee related information
Date Initiated by FirmNovember 21, 2018
Create DateDecember 22, 2018
Recall Status1 Terminated 3 on April 01, 2021
Recall NumberZ-0666-2019
Recall Event ID 81632
510(K)NumberK170317 
Product Classification System, test, human chorionic gonadotropin - Product Code DHA
ProductAlinity i Total Beta-hCG Reagent Kit, List Number 07P5121
Code Information UDI/Lot Numbers (01)00380740160616 (17)190807(10)92056UI00 / 92056UI00  
Recalling Firm/
Manufacturer
Abbott Ireland Diagnostics Division
Lisnamuck
Co. Longford Ireland
Manufacturer Reason
for Recall
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.
FDA Determined
Cause 2
Nonconforming Material/Component
ActionThe firm initiated the recall by letter on 11/21/2018. The notice explained the problem and provided instruction on how to inspect the reagent cartridges for defect. The consignee was directed to discard the defective units. The units will be replaced.
Quantity in Commerce27 units
DistributionAR, FL, GA, MD, OK, VA
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 = DHA
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