Zimmer Biomet, Inc. recalls LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS PO
See all recalls from Zimmer Biomet, Inc. →Recalled Product
LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and disability
Hazard / Issue
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: 00-5990-014-02 00-5990-015-02 00-5992-016-02
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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