Aju Pharm
8 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Aju Pharm and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-02-04FDA-DeviceClass IIStop using Aju Pharm AlternatiV+ anchors
Aju Pharm's AlternatiV+ Screw-In Anchor has been recalled due to reports of device failure. The anchor may break, bend, pull out, or the suture may break during use. Approximately 416 units were distributed in California and Puerto Rico.
- 2026-02-04FDA-DeviceClass IIStop using Aju Pharm AlternatiV+ Max anchors
Aju Pharm's AlternatiV+ Max Knotless Anchor surgical device has been recalled due to reports of failure, including anchor breakage, bending, and pulling out during use. The issue affects all lots of models 20KPN4751 and 20KPN5501 distributed in California and Puerto Rico.
- 2026-02-04FDA-DeviceClass IIStop using Aju Pharm suture anchors
Aju Pharm's Genesis Push-In Suture Anchor has been recalled due to reports of device failure during use, including the anchor breaking, bending, or pulling out, as well as suture breakage. About 200 units were distributed nationwide in California and Puerto Rico.
- 2026-02-04FDA-DeviceClass IIStop using Genesis Knotless Anchor devices
Aju Pharm Co., Ltd. is recalling Genesis Knotless Anchor surgical devices due to reports of device failure. The anchor can break, bend, pull out of tissue, the suture can break, or the packaging can break during handling or use.
- 2026-02-04FDA-DeviceClass IIStop using Genesis Dual Thread Screw-In Anchor
Aju Pharm Co., Ltd. is recalling Genesis Dual Thread Screw-In Anchor devices (Models 10N47502 and 10N55002) due to reports of failure during use. The anchor may break, bend, pull out, or cause the suture to break.
- 2026-02-04FDA-DeviceClass IIStop using Genesis Screw-In Anchor devices
Aju Pharm Co., Ltd. is recalling Genesis Screw-In Anchor devices due to reports of failure, including anchor breakage, bending, pull-out, suture breakage, and packaging damage. The recall affects models 10B45003, 10B55003, and 10B65003 distributed nationwide in California and Puerto Rico.
- 2026-02-04FDA-DeviceClass IIStop using Aju Pharm Fixone Biocomposite Anchor
Aju Pharm's Fixone Biocomposite Anchor has been recalled due to reports of device failure, including anchor breakage, bending, pulling out, suture breakage, and packaging damage. The recall affects 1,088 units distributed in California and Puerto Rico. No injuries have been reported to date.
- 2026-02-04FDA-DeviceClass IIStop using Aju Pharm Fixone Hybrid Anchor
Aju Pharm's Fixone Hybrid Anchor, a surgical device, has been recalled due to reports of device failure. Problems include the anchor breaking, bending, or pulling out during use, as well as suture breakage and packaging damage. This affects 233 units distributed in California and Puerto Rico.
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