FDAFDA · Food and drugs·Recall number Z-1035-2022
K-Wire, 1.35 mm x 170 mm
Published May 11, 2022 · Recall initiated: March 25, 2022
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
Products do not meet length and diameter specifications.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Arthrex, Inc.
- Distributor
- Worldwide distribution - US Nationwide distribution in the states of OH, TN, MO, LA, IA, AZ, PA, NY, OR and the countries of to Belgium, Egypt, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Portugal, and Spain.
- Lot
- Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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