FDAFDA · Food and drugs·Recall number Z-0150-2015
APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies, in particular for the ulna.
Published November 5, 2014 · Recall initiated: October 1, 2014
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
A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to three (3) complaints of breakage of the temporary tension bolt.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medartis, Inc.
- Distributor
- US Nationwide Distribution in the states of WV, IL, CT, AZ, and WA.
- Lot
- Part no. A-2791.05, lot no. 14125026
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.