Reported Nov 14, 2018 · Terminated
DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile…
DT MedTech, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: DT MedTech, LLC · 110 West Rd Ste 227 · Towson, MD · 21204-2341
Is this the product you have?
- DT Medical -Hintermann Series H3 Poly Inlay
- Size 3 5mm Part Number300305 components are prostheses for a mobile bearing ankle joint
- Lot codes and dates
- LotAAADP
- Amount recalled
- 54 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
Incorrect package labeling identifying the device
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new DT MedTech, LLC recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.