Non-Sterile Double DIN to DIN Y Connector recalled over sterility concerns
- Recall date
- January 20, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Molded Products Inc recalls Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the h…
- Recall number
- Z-1679-2017
- FDA classification
- Class II
- Brand / firm
- Molded Products Inc
- Sold / distributed
- Product was distributed to Ontario, Canada.
Why it was recalled
A customer relayed a complaint of a leaking dialysis tubing connector.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
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