Device recalls

VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the…

Ortho-Clinical Diagnostics, Inc. · The results generated by the VITROS Immunodiagnostic Products Vitamin B12 Range Verifier Lot# 1200 RV Level 2 may cause range verification failure. The issue i…

Open, ClassifiedNonconforming Material/ComponentZ-2019-2024
Open FDA's page for this record
Cfres ID
207931
Product res number
Z-2019-2024
Event date initiated
2024-05-08
Event date posted
2024-06-04
Recall status
Open, Classified
Res event number
94650
Product code
JJX
Code info
UDI-DI: 10758750000937 Lot Number: 1200 Exp. Date: 30-Sep-2024
Firm FEI number
1000136573
Recalling firm
Ortho-Clinical Diagnostics, Inc.
Address 1
100 Indigo Creek Dr
City
Rochester
State
NY
Postal code
14626-5101
Additional info contact
Mr. Joe Falvo 585-453-3000
Root cause description
Nonconforming Material/Component
Product quantity
76 units
Distribution pattern
Worldwide - US Nationwide and the country of Columbia.
Product description

VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used for the quantitative measurement of vitamin B12 - Product Code: 6800872

Reason for recall

The results generated by the VITROS Immunodiagnostic Products Vitamin B12 Range Verifier Lot# 1200 RV Level 2 may cause range verification failure. The issue is detectable by the user when the product fails to meet the required range during processing of RV Level 2 of this lot. There is a potential for a delay in patient test results should the user have a need to switch to an alternate method of range verification including use of an alternate lot. As this issue affects the upper limit range verification, there is no impact to VITROS Immunodiagnostic Products Vitamin B12 assay performance. Were the assay to not perform as expected, the failure would be detectable by Quality Control. Past patient sample results are unaffected, and no review of reported results is required.

Action

QuidelOrtho issued IMPORTANT PRODUCT CORRECTION NOTIFICATION (Ref. CL2024-123) to Distributors and End-Users via FedEx overnight courier and/ or electronically. Letter states reason for recall, health risk and action to take: " Discontinue using, render unusable, and discard your remaining inventory of VITROS Vitamin B12 Range Verified, Lot 1200. QuidelOrtho will replace or credit your account. Indicate quantities to be replaced or credited via the Confirmation of Receipt form. " Complete the enclosed Confirmation of Receipt form no later than May 14, 2024. " Please forward this notification if the affected product was distributed outside of your facility. If you have further questions, please contact the Global Services Organization at 1-800-421-3311.

Harmonized identifiers (openFDA)
Device name
Single (Specified) Analyte Controls (Assayed And Unassayed)
Medical specialty description
Clinical Chemistry
Regulation number
862.1660
Device class
1
K number
K101365, K962573, K003772, K791957, K031890, K926095, K112653, K013130, K953097, K970527, K001443, K990162, K093700, K092993, K122141, K772285, K143026, K924862, K904306, K030065, K083549, K981281, K851079, K822698, K060510, K040025, K050100, K060133, K150132, K092848, K121084, K090943, K050983, K022491, K955796, K042837, K935606, K970452, K092169, K940577 +453 more
Registration number
3001452053, 3003610890, 3002637618, 9612316, 3009491259, 1319681, 3010152370, 3014607865, 3013059683, 1616487, 8021924, 3004145393, 3009129531, 9611444, 3011420269, 3003902721, 3004152597, 8043909, 9681576, 3003982601, 3002806944, 3013223546, 3005529799, 1450743, 1181121, 2954323, 1832216, 3005393828, 3003559191, 3007088335, 3007363438, 3011213605, 3033967997, 3016438761, 3012494290, 3007662974, 3008344661, 2155, 9610099, 3005621222 +234 more
FEI number
3001452053, 3003610890, 3002637618, 3003400058, 3009491259, 3010152370, 3014607865, 3013059683, 1616487, 3004145393, 1000220650, 3001644026, 3009129531, 3011420269, 1000305841, 3003902721, 3004152597, 3003982601, 3004525092, 3002806944, 3004445302, 3013223546, 3005529799, 3002808212, 1450743, 1181121, 1832216, 3005393828, 3003559191, 3011213605, 3033967997, 3002806559, 3012494290, 3016438761, 3008344661, 2155, 3007662974, 3003572099, 3003355251, 3003419906 +234 more
Wholesale access for licensed clinicians.

Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.