FDAFDA · Food and drugs·Recall number Z-0969-2013
Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing.
Published March 27, 2013 · Recall initiated: June 19, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The recalled product leaks at the connection site.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Molded Products Inc
- Distributor
- Distributed to one customer in Michigan.
- Lot
- Lot numbers: 80106 and 80106b
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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