medical MODERATE Updated 2026-08-26

Intersurgical Inc recalls One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oro

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Recalled Product

One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.

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Hazard / Issue

Devices could potentially be occluded or partially occluded.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: REF: 1000035; Single Unit UDI: 5030267049844; Case UDI: 05030267044528; Lot No. 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565.

✅ 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 One-Piece Guedel Airway, size →

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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