FDA Recall Open, Classified

VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled Calibrator tube (1 per level: C1 - green, C2 - yellow, C3 - red).

Recall: Z-2142-2024 · Initiated March 1, 2024

Recall

Recall Number
Z-2142-2024
Event Number
94679
Firm
Ortho-Clinical Diagnostics, Inc.
FEI Number
1000136573
Product Code
LOM
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
March 1, 2024
Posted
June 13, 2024
Address
100 Indigo Creek Dr, Rochester, NY, 14626-5101

Description

VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled Calibrator tube (1 per level: C1 - green, C2 - yellow, C3 - red).

Reason

Potential for positively biased results due to signal reduction over shelf life.

Action

Consignees were mailed an URGENT PRODUCT CORRECTION NOTIFICATION, dated 5/14/24. In this notice consignees are instructed to discontinue using, render unusable, and discard affected product. The provided notification is to be retained and posted by each VITROS System until the issue has been resolved; copies of the recall notification are to be forwarded if affected product was distributed outside your facility. Consignees are to complete and return the provided Confirmation of Receipt form no later than 5/22/24. Consignees with any questions are to contact Quidel Ortho's Global Services Organization at 1-800-421-3311.

Distribution

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MI, MT, NC, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WI, WV and the countries of Bermuda, Colombia, Singapore.

Quantity

481 units