CLASS II Drug recall · Reported 25 Dec 2013 · FDA Enforcement Report

Carbon Dioxide, USP, Medical Gas recalled by Airgas Medical Services

Airgas Medical Services is recalling Carbon Dioxide, USP, Medical Gas, distributed in Arkansas, Kansas, Missouri. The recall was initiated on 6 Nov 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNDC 11054-002 Lot # TY00A260A Size G and H Part number 835148
Quantity recalled264 cylinders

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-366-2014
FDA event ID
66929
Recalling firm
Airgas Medical Services, Radnor, PA
Classification
Class II
Status
Terminated
Recall initiated
6 Nov 2013
FDA classified
13 Dec 2013
Reported
25 Dec 2013
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Other Reasons

Timeline

6 Nov 2013Recall initiated by company
13 Dec 2013Classified by FDA+37 days
25 Dec 2013Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Labeling: Not Elsewhere Classified; Due to an error in the manufacturing procedure, a cylinder in liquid withdrawal service was not marked Syphon Tube indicating liquid withdrawal and shipped as a gas withdrawal cylinder.

Product as listed by the FDA

Carbon Dioxide, USP, Medical Gas, Rx only, Non Flammable Gas 2, in 50 lbs steel cylinders, Distributed by AIRGAS USA, LLC Radnor, PA

Where it was distributed

Kansas, Missouri, and Arkansas.

ArkansasKansasMissouri

Questions about this recall

Why was it recalled?

Labeling: Not Elsewhere Classified; Due to an error in the manufacturing procedure, a cylinder in liquid withdrawal service was not marked Syphon Tube indicating liquid withdrawal and shipped as a gas withdrawal cylinder.

Which lots are affected?

NDC 11054-002 Lot # TY00A260A Size G and H Part number 835148

Where was it sold?

Kansas, Missouri, and Arkansas.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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Other Carbon Dioxide recalls

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