Aju Pharm Co., Ltd. 2026-02-04 Health serious FDA
Health · FDA · Recall #FDA-Z-1171-2026
Genesis Push-In Suture Anchor Recall
Issued February 4, 2026 · Aju Pharm Co., Ltd.
In February 2026, Aju Pharm Co., Ltd. recalled the Genesis Push-In Suture Anchor, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
What you should do
- 1 Stop using Genesis Push-In Suture Anchor right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Aju Pharm Co., Ltd. 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
- Aju Pharm Co., Ltd.
- Category
- Health
- Recall date
- February 4, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of CA & PR.
- Recall number
- FDA-Z-1171-2026
- Made in
- Korea (the Republic of)
- Issuing agency
- FDA
In context
- Aju Pharm Co., Ltd. has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.