Medical DeviceFeb 17, 2016
Salter Labs T-piece Nebulizer with in-line connectors, Part number 8915-7-50 recall — FDA Z-0796-2016
Reports that the T-piece does not fit on the nebulizer.
Class IIFDA: TerminatedSalter Labs
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceSep 23, 2015
Salter Labs NebuTech Nebulizer recall — FDA Z-2781-2015
The Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.
Class IIFDA: TerminatedSalter Labs
Understanding this recall history
This page summarizes recall records in which the official source identifies Salter Labs as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.