medical MODERATE Updated 2018-03-07

Teleflex Medical recalls Rusch Greenlite MAC 1, Catalog Number 004551001. Used durin

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Recalled Product

Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.

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Hazard / Issue

The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.

Issued by

FDA

Distribution: US only
Lot/Code Info: Lot/Serial number: 1602312

✅ 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.

Looking for a safe alternative?

Search Amazon for Rusch Greenlite MAC 1, →

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View official government recall

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