Waldemar Link GmbH & Co. KG (Mfg Site) 2024-03-06 Health serious FDA
Health · FDA · Recall #FDA-Z-1219-2024
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for… Recall
Issued March 6, 2024 · Waldemar Link GmbH & Co. KG (Mfg Site)
In March 2024, Waldemar Link GmbH & Co. KG (Mfg Site) recalled the LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery
What you should do
- 1 Stop using LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Waldemar Link GmbH & Co. KG (Mfg Site) to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Waldemar Link GmbH & Co. KG (Mfg Site)
- Category
- Health
- Recall date
- March 6, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution in the states of IL, IN, FL, WA and the countries of Germany, Switzerland.
- Recall number
- FDA-Z-1219-2024
- Made in
- Germany
- Issuing agency
- FDA
In context
- Waldemar Link GmbH & Co. KG (Mfg Site) has 8 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.