United StatesHintermann Series Talar Implant, Left, Size 2 (REF 302112, Lot AACAA, DI B095302112) distributed worldwide including CA, AR, AZ, ID and countries PER and KOR is being recalled. The recall was initiated after customer complaints found the left implant packaging and labeling can contain a right implant device.
What's being recalled
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Recalling firm: DT MedTech, LLC, Mcminnville, TN, United States.
How to identify it
Lot: AACAA/ DI: B095302112
The hazard
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)