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U.S. Department of Health and Human Services

Class 2 Device Recall Helix Elite

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 Class 2 Device Recall Helix Elitesee related information
Date Initiated by FirmJune 06, 2017
Create DateMarch 01, 2022
Recall Status1 Terminated 3 on January 17, 2023
Recall NumberZ-0699-2022
Recall Event ID 89446
Product Classification Multi-analyte controls unassayed - Product Code OHQ
ProductHelix Elite" Molecular Standards: Inactivated Standard. Inactivated Respiratory Syncytial Virus A Strain Long. Target pathogens are lyophilized in a PCR compatible matrix, and stable at 2C-25C through the expiration date. Each lyophilized pellet is packaged in a single-use foil pouch. Each kit contains 5 unassayed lyophilized pellets, packaged in individual vials for ease-of-use and to avoid cross contamination.
Code Information Catalog Number: HE0028N; Lot Number: HE0028N-102-1; UDI: 10845357042023
Recalling Firm/
Manufacturer		 Microbiologics Inc
200 Cooper Ave N
Saint Cloud MN 56303-4440
For Additional Information ContactBecky Neu
320-229-7073
Manufacturer Reason
for Recall		Real-time shelf life testing failed at 24 months
FDA Determined
Cause 2		Process design
ActionMicrobiologics notified customers on about 06/06/2017 via email containing a letter. The letters indicated the affected products and instructed customers to update their records with the corrected expiration date, which was provided for each affected lot.
Quantity in Commerce1 unit
DistributionWorldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.
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.
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