Accula SARS-CoV-2 Test, REF: COV4100
Recall
- Recall Number
- Z-1009-2022
- Event Number
- 90013
- Firm
- MESA BIOTECH, INC
- FEI Number
- 3013026082
- Product Code
- QJR
- Status
- Open, Classified
- Root Cause
- Material/Component Contamination
- Initiated
- April 6, 2022
- Address
- 6190 Cornerstone Ct E, Ste 220, San Diego, CA, 92121-4701
Description
Accula SARS-CoV-2 Test, REF: COV4100
SARS-CoV-2 Test has an increased potential for false positive results, which may lead to a delay in correct diagnosis and treatment.
On 04/06/22, recall notices were mailed to customers. Customers were informed that the reliability of negative test results is not affected. Customers with affected devices were asked to do the following: 1. Discontinue use of any affected product immediately 2. All affected product must either be returned or discarded. Replacement product will be provided for all returned and discarded product upon receipt of Customer/Distributor Response Sheet. 3. Notify all impacted users in your facility. If you have shipped any of these lots outside of your facility, you must notify those customers or facilities of this voluntary recall. 4. Complete and return the Customer/Distributor Response Sheet, which can be emailed to [email protected] Customers with questions are encouraged to contact the recalling firm at: +1-858-800-4929, or 1-800-955-6288, option 2.
US Nationwide distribution in the states of CA, TX, MA, NY, FL, NC, NJ, GA, CO, HI, PA, WA, NY, VA, MD, KY, WI, IL, PR, ND, MI, TN, AZ, UT.
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