Health & Personal Care Recalls

1,814 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model SL Implant Component Recalled for Detachment Risk (2026)

Waldemar Link recalled 44 Endo-Model SL implant components sold through multiple distributors worldwide, including 1 unit in the United States. The bushing could detach from the screw shaft because of a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Waldemar Link for returns or replacements.

Waldemar Link
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model SL Connection Component Recalled for 31 Units (2026)

Waldemar Link recalled 31 Endo-Model SL Connection Components incl. PE-Plateau sold worldwide, including New Jersey. The device bears a risk that the bushing could detach from the screw shaft due to a longitudinal fracture. Clinicians and patients should stop using the device immediately and follow manufacturer instructions.

Waldemar Link
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model 15-0027/12 Implant Recall 2026 for Detachment Risk

Waldemar Link recalled 1 unit of Endo-Model Replacement Plateau implant component distributed worldwide, including New Jersey. The defect involves a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Waldemar Link GmbH & Co. KG
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Implant Recall: Endo-Model Replacement Plateau 15-8521/09 Looks to Detach from Screw (

Waldemar Link GmbH & Co. KG recalls 8 units of Endo-Model Replacement Plateau worldwide after a reported risk that a bushing could detach from the screw shaft due to a longitudinal fracture. The recall also covers US distribution in New Jersey. Health authorities have classified the risk as high. Patients and healthcare providers should stop using the device immediately and follow recall guidance.

Waldemar Link GmbH & Co. KG
The potential
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Health & Personal Care
HIGH
FDA DRUG

Rising Pharmaceuticals Recalls Furosemide Tablets for Contamination Risk

Rising Pharmaceuticals recalled 4,212 bottles of Furosemide Tablets on January 10, 2026. The recall stems from the discovery of a foreign substance in the medication. Consumers should stop using the product immediately and seek guidance from their healthcare provider.

FUROSEMIDE
Presence of
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Health & Personal Care
HIGH
FDA DEVICE

Medartis AG Recalls 2.5 TriLock Screw 16mm HD7 1/Pkg Worldwide (2026)

Medartis AG recalled the 2.5 TriLock Screw 16mm HD7, 1/Pkg, sold worldwide through medical distributors including the US states of Indiana and Pennsylvania. The recall stems from a mix-up between 2.5mm and 2.8mm outer diameter screws. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

Medartis
Mix up
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Health & Personal Care
HIGH
FDA DEVICE

FUJIFILM Healthcare Recalls X-ray Generator Over Fire Hazard

FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.

FUJIFILM Healthcare Americas
It was
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiopulmonary Recalls Venous Bubble Sensor Due to Cable Risk

Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.

Maquet Cardiopulmonary Gmbh
Internal investigations
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Dialysis Kits Over Risk of Seal Failure

Medline Industries recalled 150 dialysis convenience kits on January 8, 2026, due to silicone seal defects. Affected kits may obstruct fluid paths and risk exposure to biological contaminants.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DEVICE

Medline Dialysis Kits Recalled Over Silicone Seal Issues

Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Tego Connectors Over High Risk of Fluid Leakage

Medline Industries recalled 1,212 kits containing Tego Connectors on January 8, 2026. The recall stems from issues with silicone seals that may cause occluded fluid paths. Users may experience delays in therapy or exposure to contaminants due to this defect.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Kits Recalled Due to High Hazard Risk

Medline Industries recalled 516 medical kits on January 8, 2026, due to issues with Tego Connectors. The silicone seal may tear or dome, posing a high risk of therapy interruption and exposure to contaminants. Healthcare providers must stop using these devices immediately and follow recall instructions.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DEVICE

Medline Dialysis Kits Recalled Over Risk of Fluid Leakage

Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Dialysis Dressing Change Kits Over High Hazard

Medline Industries recalled 31,848 dialysis dressing change kits on January 8, 2026. The recall follows reports of defective silicone seals on Tego Connectors that may occlude fluid paths. This defect can delay therapy and expose patients to biological contaminants.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)

Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.

Olympus
Mis-wired component-the
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Convenience Kits Over Sterility Concerns

Medline Industries recalled 9,720 convenience kits on January 7, 2026, due to sterilization calibration issues. The affected products may not meet sterility assurance levels. Patients and healthcare providers should stop using these kits immediately.

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Convenience Kits Over Sterility Issues

Medline Industries, LP recalled 684 medical convenience kits on January 7, 2026. The recall affects the LVAD Driveline Tray and the KIT Surg Onc Insert Cent. Venou due to calibration issues impacting sterility. Health providers and patients should stop using these products immediately.

Medline Industries, LP
Medline has
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Category Statistics

Total Recalls
1,814
Pages
91