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United States·US-MF-000007934
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 30, Spur Drive, El Paso, United States
- Website
- myairlife.com
- —
- —
- [email protected]
- Phone
- +1-269-873-0502
- PRRC Contact
- Robert Yamashita
- EUDAMED SRN
- US-MF-000007934
- FDA FEI Number
- 3004748541
- DUNS Number
- 022721133
Catalogue (988)
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jun 25, 2014 | Z-2093-2014 | — | terminated | The case label correctly states partial rebreather but the insert label incorrectly states non-rebreather. |
| Nov 1, 2013 | Z-0360-2014 | — | terminated | It has been determined that three lots of model number 4515-15-25 CO2 Sample Line 15' tube, male Luer lock connectors may contain a 30' tube instead of the 15' length. |
| May 30, 2012 | Z-1898-2012 | — | terminated | A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector actually contained product with a female luer lock connector. |
| Dec 7, 2011 | Z-0605-2012 | — | terminated | Mis-labeling: report of cases labeled as 4707 (cannulas with male luer lock connector) actually contained 4707F (with female luer lock connectors). |
| Oct 21, 2011 | Z-0803-2012 | — | terminated | A manufacturing defect was discovered internally which indicates that in a small number of humidifier lids, the pop-off may not occur at the appropriate pressure and can result in a leak. |