FDA recall record

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 IIclassification
Z-0796-2016official record ID
Feb 17, 2016report date

Recall record at a glance

Official recordZ-0796-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSalter Labs
Report dateFeb 17, 2016
Recall initiation dateJan 5, 2016
Quantity70 units
LocationCarlsbad, CA, United States

Official product description

T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment.

Why the product was recalled

Reports that the T-piece does not fit on the nebulizer.

Distribution information

Distributed in the states of TX, NY, PA, TN, SC, and OH, and in China.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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