medical MODERATE Updated 2026-10-14

DRG International, Inc. recalls Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product De

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Recalled Product

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

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Hazard / Issue

Potential for false negative patient results.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model/Catalog Number: EIA-1826; UDI: 04048474018264; Lot# 320K046;

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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Search Amazon for Sperm Ab ELISA; →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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