Reported Feb 4, 2026 · Ongoing
Genesis Screw-In Anchor
Aju Pharm Co., Ltd.
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: Aju Pharm Co., Ltd. · Room 201, Room 207, Bl A · Seongnam, N/A · N/A
Is this the product you have?
- Genesis Screw-In Anchor
- Lot codes and dates
Model No. 10B4500310B5500310B65003All UDI CodesAll Lots
- Amount recalled
- 600 units
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
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 Aju Pharm Co., Ltd. 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.