FDA recall record

SIEMENS HEALTHCARE DIAGNOSTICS N Antiserum to Human IgG, 2mL Variant for BN II System and BN recall — FDA Z-0093-2023

N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect expectation of up to 648 mg/L for IgGU (urine) and up to 2290 mg/L for IgGC…

Class IIclassification
Z-0093-2023official record ID
Oct 26, 2022report date

Recall record at a glance

Official recordZ-0093-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSIEMENS HEALTHCARE DIAGNOSTICS Inc.
Report dateOct 26, 2022
Recall initiation dateAug 30, 2022
Quantity373 PCK
LocationTarrytown, N/A, Spain

Official product description

N Antiserum to Human IgG, 2mL Variant for BN II System and BN ProSpec System-IVD Siemens Material Number (SMN): 10446297

Why the product was recalled

N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect expectation of up to 648 mg/L for IgGU (urine) and up to 2290 mg/L for IgGC (CSF).

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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