medical MODERATE Updated 2025-08-06

Remel, Inc recalls Strep Selective II Agar, Product Number R01859

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Recalled Product

Strep Selective II Agar, Product Number R01859

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Hazard / Issue

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 848838003158; Lot Numbers: 271613

✅ 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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