T-piece Nebulizer with in-line connectors recall
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…
Why was T-piece Nebulizer with in-line connectors recalled?
Reports that the T-piece does not fit on the nebulizer.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot No. 083115, 090715, and 122815
- Product
- 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…
- Recalling firm
- Salter Labs
- Quantity
- 70 units
- Distribution
- Distributed in the states of TX, NY, PA, TN, SC, and OH, and in China.
- Recall date
- February 17, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)