⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Aju Pharm Co., Ltd.: AlternatiV+ Screw-In Anchor

Medical DevicesSource: FDA (device) · Date: 2026-02-04

Read the official notice at FDA (device) →

Share on XFacebookRedditEmail

Get alerts for Aju Pharm

Guides: Which agency handles which recall (FDA vs USDA vs CPSC vs NHTSA)

The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Aju Pharm Co., Ltd.
Product
AlternatiV+ Screw-In Anchor
Reason / hazard
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Classification
Class II
Status
Ongoing
Distribution / sold at
US Nationwide distribution in the states of CA & PR.
Recall initiated
2025-12-17
Code info
Model No. 20BN4753, 20BN5503; All UDI Codes; All Lots.
Product quantity
416 units
Voluntary mandated
Voluntary: Firm initiated
City
Seongnam
State
N/A
Country
Korea (the Republic of)
Event id
98312
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.