Health & Personal Care
HIGH
FDA DEVICE
Vascutek Gelsoft Plus and Gelweave Vascular Prostheses Recalled for Shelf-Life Label Error (37,430,
Vascutek
Gelatin sealed
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
23
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DRUG
Imprimis NJOF Recalls Intraocular Injection Due to Glass Particles
Presence of particulate matter - Glass like particles.
Imprimis NJOF
Presence of
HIGH
CPSC
Plantimex Recalls Mamisan Ointment Due to Child Poisoning Risk
MiramarLab, of Doral, Florida
The ointment
Health & Personal Care
HIGH
FDA DEVICE
Rifton Recalls E-Pacer Gait Training Device Over Fraying Risk
Rifton Equipment recalled 470 E-Pacer gait training devices on December 18, 2025. The body support strap may fray, posing a risk to users. Health care providers and patients must stop using the device immediately.
Community Products
Potential for
MEDIUM
CPSC
TopHomer Pool Drain Covers Recalled Over Drowning Hazards
TopHomer recalled pool drain covers on December 18, 2025, due to serious entrapment and drowning hazards. The recall affects 8-inch drain covers sold on Amazon. Consumers should immediately stop using the products and seek refunds.
TopHomer Pool Drain Covers
The recalled
Health & Personal Care
HIGH
FDA DEVICE
Rifton Equipment Recalls TRAM Lift Device Over Strap Hazards
Potential for fraying on the body support strap.
Community Products
Potential for
Health & Personal Care
HIGH
FDA DRUG
Imprimis NJOF Recalls Intraocular Injection Over Glass Particles Hazard
Imprimis NJOF, LLC recalled 596 boxes of intraocular injections on December 18, 2025. The recall affects products due to the presence of glass-like particles. Consumers should stop using the product immediately and contact their healthcare provider.
Imprimis NJOF
Presence of
Health & Personal Care
HIGH
FDA DRUG
Imprimis NJOF Recalls Intraocular Injection Over Glass Particles
Presence of particulate matter - Glass like particles.
Imprimis NJOF
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Rifton Equipment Recalls Low Base TRAM Due to Fraying Hazard
Potential for fraying on the body support strap.
Community Products
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Wilson-Cook Medical Recalls Bipolar Sphincterotomes Due to Hazard
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.
Wilson-Cook Medical
Due to
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls Dual Thread Screw-In Anchors Over Device Failures
Aju Pharm Co. recalled 400 Dual Thread Screw-In Anchors on December 17, 2025. The recall follows reports of device failures including breakage and pull-out incidents. Healthcare providers and patients should stop using these devices immediately.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls Biocomposite Anchor Due to Device Failures
Aju Pharm Co. recalled 1,088 units of its Fixone Biocomposite Anchor on December 17, 2025, due to serious device failures. Reports include anchor breakage, bending, and suture breakage. Healthcare providers and patients must stop using the device immediately.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls Screw-In Anchor Due to Device Failure Risks
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Co. Recalls Genesis Push-In Suture Anchor Due to Device Failures
Aju Pharm Co. recalled 200 units of the Genesis Push-In Suture Anchor on December 17, 2025. Users reported serious device failures including anchor breakage and suture breakage. Consumers and healthcare providers must stop using the device immediately.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DRUG
CareFusion Recalls ChloraPrep Swabsticks Due to Sterility Concerns
CareFusion 213, LLC recalled 106,400 units of ChloraPrep Triple Swabsticks on December 17, 2025. The recall occurred due to a lack of assurance of sterility. Consumers must stop using the product immediately and contact CareFusion for guidance.
ChloraPrep
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls Screw-In Anchors Due to Device Failure
Aju Pharm Co. recalled 600 units of Genesis Screw-In Anchors on December 17, 2025. Reports indicate serious device failures, including anchor breakage and suture breakage. Healthcare providers and patients should stop using these anchors immediately.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls AlternatiV+ Max Knotless Anchor Due to Device Failures
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls Genesis Knotless Anchor Due to Device Failure
Aju Pharm Co. recalled 1,163 units of Genesis Knotless Anchor on December 17, 2025, after reports of device failures. Issues include anchor breakage and suture breakage. Patients and healthcare providers must stop using the device immediately.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Aju Pharm Recalls Fixone Hybrid Anchor Due to Device Failures
Aju Pharm Co. recalled 233 Fixone Hybrid Anchors on December 17, 2025, due to multiple reports of device failures. The issues include anchor breakage, bending, and suture breakage. Patients and healthcare providers must stop using the device immediately.
Aju Pharm Co.
Reports of
Health & Personal Care
HIGH
FDA DEVICE
Vortex Surgical Recalls 25GA Backflush Pouches Over Infection Risk
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
Vortex Surgical
There may
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls Medical Procedure Kits Due to Leakage Risk
Medline Industries, LP
Medline kits
Health & Personal Care
HIGH
FDA DEVICE
Medline Medical Kits Recalled Due to Suction Irrigator Hazards
Medline recalled 41,432 medical procedure convenience kits on December 16, 2025. The kits contain Stryker's Strykeflow 2 Suction Irrigators that may leak or emit vaporized saline. This defect poses a high risk of injury during medical procedures.
Medline Industries, LP
Medline kits
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls Medical Kits Due to Suction Irrigator Leak Hazard
Medline Industries, LP
Medline kits
Health & Personal Care
HIGH
FDA DEVICE
Medline Medical Kits Recalled Over Strykeflow 2 Suction Hazard
Medline recalled 4,536 medical procedure kits on December 16, 2025. The kits contain Stryker's Strykeflow 2 Suction Irrigators that may leak and emit vaporized saline. The recall affects various models used in surgeries nationwide.
Medline Industries, LP
Medline kits
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