ClearanceBrief
Recall Z-0065-2024 ยท JHI Visual, Pregnancy Hcg, Prescription Use

Universal Meditech Inc.

DiagnosUS hCG Pregnancy Serum/Urine Test Cassette Format REF 100-27

DateOct 23, 2023 (initiated May 22, 2023)
StatusOpen, Classified
ReasonUniversal Meditech Inc. was violatively distributing PrestiBio" Breastmilk Alcohol Test Strip, DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test, HealthyWiser KetoFast" Ketone Test Strips and PrestiBio" Ketone Test Strips without marketing authorization. UMI is also recall their tests because they are going out of business and would not be able to continue fulfilling any post-market responsibilities of these distributed products. UMI claims to hold 510(k)s for the other devices, purchased the intellectual property in 2015 from the previous 510(k) holder, but FDA has been unable to verify this info
Root causeOther
ActionOn 06/07/2023, the firm emailed customers to inform them of the intent of the firm to recall all products we have sold to them in the past two years; in that email, UMI has advised them to immediately stop further distribution of any product that was made by UMI. In the past few weeks, UMI has conducted a thorough investigation of their order information. We will send formal recall letters to them with all the batch information of all products they have ordered since March 2021. On 06/30/2023, the firm sent via US Certified Post, a hard copy letter of it first version of the recall notificati
Quantity1,000 cassettes
DistributionU.S.: CA, FL, IL, LA, NJ, NY, TX and WY O.U.S.: Taiwan
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K963133PS-UNIT CASSETTE/SERUM HCG
International Newtech Development, Inc., Nov 18, 1996