Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BiMobile UHMWPE Liner: ID-28mm/OD-54mm Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The internal labeling included with these implants may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Waldemar Link GmbH & Co. KG (Mfg Site) directly.
Affected Products
BiMobile UHMWPE Liner: ID-28mm/OD-54mm, Reference Number 184-260/04 The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intended for cemented and cementless use.
Quantity: 31
Why Was This Recalled?
The internal labeling included with these implants may include incorrect part numbers and could result in these incorrect labels being added to patient records.
Where Was This Sold?
This product was distributed to 8 states: AZ, FL, GA, LA, MI, MN, TX, WA
About Waldemar Link GmbH & Co. KG (Mfg Site)
Waldemar Link GmbH & Co. KG (Mfg Site) has 62 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report