Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TaperFit Stem Recalled by Corin Ltd Due to Some of the devices did not pass fatigue...
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 Corin Ltd directly.
Affected Products
TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
Quantity: 1
Why Was This Recalled?
Some of the devices did not pass fatigue testing.
Where Was This Sold?
This product was distributed to 1 state: NJ
About Corin Ltd
Corin Ltd has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report