Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66929

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 06, 2013
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Airgas Medical Services

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-366-2014
Recall number
D-366-2014
Initiated
November 06, 2013
Classification
Class II
Status
Terminated
Recalling firm
Airgas Medical Services
Quantity
264 cylinders

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
error in the manufacturing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

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

Distribution pattern

Kansas, Missouri, and Arkansas.