Recall

Could cause harm

Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96…

Potential for false negative patient results.

FDA enforcement record

What to do

Does your product match this recall?

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  1. 1Compare the product, size and lot or date code with this notice.
  2. 2If your product matches, stop using it and follow the official recall instructions.
  3. 3Read the official notice for return, refund or disposal instructions.

Recall details

Firm
DRG International, Inc.
Status
Posted
Reported
Oct 2, 2026
Started
Jul 2, 2026
Where sold
Worldwide - US Nationwide distribution in the state of NJ and the countries of Azerbaijan, Belgium, Czech Republic, Germany, Hungary, India, Italy, Kuwait, Russia, Spain, Ukraine.
Quantity
211
Notice number
Z-0082-2027

Lots, UPC, dates

Model/Catalog Number: EIA-1826; UDI: 04048474018264; Lot# 320K046;

Agency wording

Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);

Source: FDA enforcement. This is not medical advice. Compare your package codes before you act.