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Helix Elite Molecular Standards: Inactivated Standard recallZ-0954-2022 · Microbiologics Inc · initiated Mar 24, 2022

Terminated

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Microbiologics Inc or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

QC process was not adequate for the specification range.

FDA root cause category: Process control

What the company is doing

A customer letter, dated 03/24/2022, was emailed to the impacted consignee. The consignee is instructed to destroy the product as it is now past its updated expiration date. The consignee is asked to complete the response form and submit to the recalling firm.

Recall details

Recall number
Z-0954-2022
Status
Terminated
Initiated by the company
Mar 24, 2022
Recalling firm
Microbiologics Inc
Quantity
1 ea
Product code
OHQ
Distribution
US Nationwide distribution in the state of TX.

Product description

Inactivated macrolide and quinolone-resistant Mycoplasma genitalium

Code information (models, lots, serial numbers)

Catalog HE0069N; Lot HE0069-02-1 UDI: 10845357043990

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Sources and updates

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