medical MODERATE Updated 2025-02-26

Remel, Inc recalls remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100

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Recalled Product

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

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Hazard / Issue

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 848838003691, Lot Number 213926, exp. 2025-02-24

✅ 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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