Class II U.S. Food and Drug Administration

Intersurgical Inc One-Piece Guedel Airway, size 000, ISO 3.5 recall: Devices could potentially be occluded or partially occluded

Recall published 2 months ago

Devices could potentially be occluded or partially occluded.

The hazard: Device safety concern

The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

What the notice says: Devices could potentially be occluded or partially occluded.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-2953-2026
Published
August 26, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Intersurgical Inc
Product type
Medical devices
Units affected
1,575 units
Distribution
Nationwide
Made in
United States
Lot / code info
REF: 1000035; Single Unit UDI: 5030267049844; Case UDI: 05030267044528; Lot No. 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565.
UPC codes
5030267049844, 05030267044528

Products covered by this recall

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

Check your product

The notice names 10 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 5030267049844
  • 05030267044528

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 32190425
  • 32213076
  • 32221283
  • 32307261
  • 32317627
  • 32321305
  • 32513841

Model or item number

On the rating label, the box or the instruction sheet.

  • 1000035

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Intersurgical Inc — The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. Ask the supplier or clinic that provided it what the remedy is in your case.
  3. If you are a facility, quarantine affected stock and log the correction.
  4. Report device problems to the FDA through MedWatch.

Who pays for a device recall

The manufacturer funds the remedy. The practical question is usually which link in the chain executes it.

  • If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.
  • Ask for written confirmation that the remedy was applied to your serial number. That is what an insurer or a future clinician will want to see.
  • If you bought it yourself online or from a pharmacy, go to the manufacturer’s recall page rather than the retailer; device claims are handled centrally.
  • Where the remedy is a software update, there is nothing to claim, but do confirm the version changed afterwards.

Company contact: Intersurgical Inc — 5010 Campuswood Dr Ste 102, East Syracuse, NY, 13057-1561

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Intersurgical Inc medical devices recalled?

Devices could potentially be occluded or partially occluded. Devices could potentially be occluded or partially occluded.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 5030267049844, 05030267044528; lot code 32190425, 32213076, 32221283; model number 1000035. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.

Where was the recalled product sold?

It was distributed nationwide.

Related recalls