Data Foundry

Drug recalls 2016

UN1002 Air — Class III drug recall D-0782-2016

Terminated recall by Praxair Inc., reported 2016-04-06, distributed nationwide. CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.

Recall numberD-0782-2016
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPraxair Inc., Danbury, CT, United States
Recall initiated2015-09-16
Classified2016-03-28
Reported by FDA2016-04-06
Terminated2016-05-10
DistributedNationwide (US)
Quantity127 cylinders
Reason classescgmp
Lot numbersP411517501, P411517601, P411517701, P411518001, P411518101, P411518201, P411518202, P411518301, P411518701, P411518801, P411518901, P411519101, P411519401, P411519601, P411519602, P411519701, P411520101, P411520301, P411520401, P411520901, P411521001, P411521002, P411521101, P411521201, P411521501, P411521601, P411521701, P411521801, P411521901, P411522201, P411522401, P411522501, P411522901, P411523001, P411523101, P411523201, P411523301, P411523601, P411523701, P411523801 and 3 more

Product

UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.

Reason for recall

CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0782-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.