PlainRecalls
FDA Devices Moderate Class II Ongoing

BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack

Reported: May 17, 2023 Initiated: February 28, 2023 #Z-1572-2023

Product Description

BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack

Reason for Recall

APLS IgM reagent kits were packaged with the incorrect conjugate, which could lead to an increase in false-positive and false-negative results.

Details

Units Affected
932 Reagent Packs
Distribution
US Nationwide distribution including in the states of AL, AR, AZ, CA, CT, FL, HI, IL, IN, KS, KY, LA, MI, MO, NC, ND, NE, NJ, NM, NY, OH, OK, PR,SC, TN, TX, UT, VT.
Location
Redmond, WA

Frequently Asked Questions

What product was recalled?
BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack. Recalled by Bio-Rad Laboratories, Inc.. Units affected: 932 Reagent Packs.
Why was this product recalled?
APLS IgM reagent kits were packaged with the incorrect conjugate, which could lead to an increase in false-positive and false-negative results.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 17, 2023. Severity: Moderate. Recall number: Z-1572-2023.