FDAFDA · Food and drugs·Recall number Z-0308-2020
PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00234700118 00234700206 00234700208 00234700210 00234700212 00234700214 00234700216 00234700218 00234703104 00234703106 00234703108 00234703204 00234703206 00234703208
Published November 13, 2019 · Recall initiated: October 10, 2019
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
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Zimmer Biomet, Inc.
- Distributor
- Distributed nationwide.
- Lot
- All product manufactured prior to January 2014.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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