Exact FDA event identifier

Event 61917

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

Event summary

Timeline bucket: May 04, 2012
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Linde Gas LLC

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

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

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

LifeGas OXYGEN COMPRESSED UN1072 USP, Distributed by: Linde

D-1383-2012

Recall number: D-1383-2012
Initiated: May 04, 2012
Classification: Class II
Status: Terminated
Recalling firm: Linde Gas LLC
Quantity: 283 cylinders

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0

CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: The pressure gages, vacuum gages, and thermometer had surpassed the calibration expiry period, which may have resulted in overfill/underfill of oxygen cylinders.

Code information

LOT#: 117H201 LOT#: 117H202

Distribution pattern

Distributed only within Ohio. No Federal Government, foreign or Canadian consignees received product.