FDA Drug recall D-0423-2015
AIR COMPRESSED, Medical Air, USP, Rx Only
- FDA Drug
- Class III
- terminated
- Published 2015-04-01
On 2015-04-01 the FDA classified a Class III recall of AIR COMPRESSED, Medical Air, USP, Rx Only by Matheson, citing failed Impurities/Degradation Specification; out of specification results for carbon dioxide.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0423-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-03-10 |
| Published | 2015-04-01 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Matheson |
| Distribution | MI, WI |
Product
AIR COMPRESSED, Medical Air, USP, Rx Only. Matheson Tri-Gas, Inc., 150 Allen Road, Basking Ridge, NJ 07920. Available in A) E or 22 cu ft cylinder, NDC: 55037-302-09; B) 40 cu ft cylinder, NDC: 55037-302-10; C) 200 cu ft cylinder, NDC: 55037-302-15; D) 220 cu ft cylinder, NDC: 55037-302-16; E) 300 cu ft cylinder, NDC: 55037-302-18, 55037-302-19, 55037-302-20.
Reason
Failed Impurities/Degradation Specification; out of specification results for carbon dioxide
Identifiers
| ndc | 55037-302-01 |
|---|---|
| ndc | 55037-302-02 |
| ndc | 55037-302-03 |
| ndc | 55037-302-04 |
| ndc | 55037-302-05 |
| ndc | 55037-302-06 |
| ndc | 55037-302-07 |
| ndc | 55037-302-08 |
| ndc | 55037-302-09 |
| ndc | 55037-302-10 |
| ndc | 55037-302-11 |
| ndc | 55037-302-12 |
| ndc | 55037-302-13 |
| ndc | 55037-302-14 |
| ndc | 55037-302-15 |
| ndc | 55037-302-16 |
| ndc | 55037-302-17 |
| ndc | 55037-302-18 |
| ndc | 55037-302-19 |
| ndc | 55037-302-20 |
| code_info | A) Lot #: BAHC564281A, BAHC564281B, BAHC546288A, BAHC564288B, BAHC546288C, BAHC546288D, BAHC546288E, BAHC564307A, BAHC5…A) Lot #: BAHC564281A, BAHC564281B, BAHC546288A, BAHC564288B, BAHC546288C, BAHC546288D, BAHC546288E, BAHC564307A, BAHC564314A, BAHC564329A. BAHC564329B, BAHC564329C, BAHC564329D, BAHC564329E, BAHC564344A, BAHC565005A, BAHC565006A, BAHC565013A, BAHC565015A, BAHC565015B, BAHC565015C, BAHC565015D, BAHC565029A, BAHC565035A. BAHC565035B, BAHC565035D; B) Lot #: BAHC564282A, BAHC564296A, BAHC564303A, BAHC564344A, BAJC565016A, BAHC565034A, BAHC565043A, BAHC565054A; C) Lot #: BAHC564269A, BAHC564275A, BAHC564282A, BAHC564288A, BAHC564296A, BAHC564303A, BAHC564308A, BAHC564317A, BAHC564324A, BAHC564329A, BAHC564338A, BAHC564344A, BAHC564351A, BAHC565016A, BAHC565020A, BAHC565028A, BAHC565043A, BAHC565054A; D) Lot #: BAHC564365A; E) Lot #: BAHC564269A, BAHC564275A, BAHC564279A, BAHC564282A, BAHC564290A, BAHC564296A, BAHC564303A, BAHC564308A, BAHC564317, BAHC564324A, BAHC564329A, BAHC564350A, BAHC564356A, BAHC564365A, BAHC565005A, BAHC565006A, BAHC565013A, BAHC565020A, BAHC565029A, BAHC565042A, BA |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0423-2015%22
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