Osom Ultra hCG Combo Test- IVD immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in serum or urine for the early confirmation of pregnancy. Model/Catalog Number: 1004
Recall
- Recall Number
- Z-0259-2025
- Event Number
- 95439
- Firm
- Princeton Biomeditech Corp
- FEI Number
- 2246703
- Product Code
- JHI
- Status
- Open, Classified
- Root Cause
- Process change control
- Initiated
- August 23, 2024
- Posted
- October 30, 2024
- Address
- 4242 US Highway 1, Monmouth Junction, NJ, 08852-1905
Description
Osom Ultra hCG Combo Test- IVD immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in serum or urine for the early confirmation of pregnancy. Model/Catalog Number: 1004
This recall was initiated due to customer complaints of false negative of hCG test results when running patient urine samples. Use of the above listed product lot may result in false negative results. An end user reported that the OSOM Ultra hCG Combo Test, lot 563L13, produced false negative test results from 2 patient urine samples as confirmed by quantitative hCG and ultrasound. During further root cause testing and investigation, an additional 6 devices were found to produce false negative test results from hCG positive samples.
PBM notified the Distributor Sekisui Diagnostics on 8/23/24 via email. The sent an "URGENT PRODUCT RECALL NOTICE" dated 8/30/24 to customers. Sekisui Diagnostics issued a recall notice on 9/6/24 to its customers. PBM Letter states reason for recall, health risk and action to take: Stop distribution or use of OSOM Ultra hCG Combo Test lot 563L13. " If you have further distributed this product, please identify your customers, and notify them at once of this product recall. This recall should be carried out to the user level. Your notification to your customers may be enhanced by including a copy of this recall notification letter. " Quarantine and return any kits from the listed lots, (1) currently in your inventory, and (2) returned from your customers. " Indicate the quantity returned on the attached CONFIRMATION OF NOTIFICATION form, and follow the instructions to complete, even if you do not have any affected product remaining in your inventory. Complete, sign and return the CONFIRMATION OF NOTIFICATION form to the email provided by the date indicated on the form. Please note replacement product equivalent to the quantity of products you returned from the affected lot will be processed once the CONFIRMATION OF NOTIFICATION form has been received. If you have any questions, call PBM Technical Services at Tel 1-732-274-1000 or E-mail .
US Distribution to MO only.
1,860 kits (50,220 test devices)