Health & Personal Care Recalls

1,620 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

Merit Medical CentrosFLO Hemodialysis Catheters Recalled for 35,591 Units (2026)

Merit Medical Systems has issued an active recall affecting 35,591 CentrosFLO Hemodialysis Catheters sold worldwide. The recall centers on a 16F dual-valved splittable sheath introducer that may fail to split as intended. This failure can cause hemorrhage, foreign-body retention, and procedure delays. Healthcare providers should stop using the device and follow Merit Medical's recall instructions.

Merit Medical Systems
16F dual-valved
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical 16F Dual-Valved Splittable Sheath Introducer Recalled for 368,264 Units Worldwide (202

Merit Medical Systems recalls 368,264 units of the 16F Dual-Valved Splittable Sheath Introducer bulk non-sterile sold worldwide. A design defect may prevent the sheath from splitting as intended, risking hemorrhage and foreign bodies. Healthcare providers should stop using the device and contact Merit Medical for instructions.

Merit Medical Systems
16F dual-valved
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical ProGuide 16F Dialysis Sheath Introducer Recalled Worldwide in 2026 (131 Units)

Merit Medical Systems recalled 131 units of the ProGuide chronic dialysis catheter introducer worldwide after a design defect could prevent the device from splitting as intended. The defect may cause hemorrhage, retained foreign bodies, and delays to procedures. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.

Merit Medical Systems
16F dual-valved
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical BioFlo DuraMax Catheter Recall 2026: 47,153 Units Worldwide

Merit Medical Systems recalled 47,153 BioFlo DuraMax Catheters distributed worldwide through medical distributors after a design defect in the 16F dual-valved splittable sheath introducer may fail to split as intended. The defect can cause hemorrhage, foreign bodies, and delays in procedures. Clinicians and patients should stop using the device immediately and follow recall instructions from Merit

Merit Medical Systems
16F dual-valved
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Health & Personal Care
HIGH
FDA DRUG

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall (2026)

Harbin Jixianglong Biotech Co. recalled semaglutide for Rx compounding use distributed nationwide to healthcare providers in the United States. The recall cites CGMP deviations and failure to complete process validation and bacterial endotoxin method validation before distribution. Healthcare providers and patients should stop using this product immediately and contact the manufacturer or their CL

Harbin Jixianglong Biotech Co.
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall 2026 — 6 Packaging Sizes

Harbin Jixianglong Biotech Co. recalled Semaglutide for Rx compounding use nationwide in the United States. The recall cites CGMP deviations and failure to complete endotoxin validation before distribution. Healthcare providers and patients should stop using the product immediately and contact the company or a healthcare provider for guidance via email.

Harbin Jixianglong Biotech Co.
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

AvKARE Recalls Amantadine HCl Capsules Over Dissolution Issues

AvKARE recalled Amantadine HCl capsules on February 13, 2026, due to failed dissolution specifications. The recall affects the 100 mg capsules, which may not dissolve properly. Consumers should stop using this product and contact their healthcare provider immediately.

AMANTADINE HCL
Failed Dissolution
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Health & Personal Care
HIGH
FDA DEVICE

Erbe USA Recalls 2,408 Flexible Cryoprobes for Surgery Over Rupture Risk (2026)

Erbe USA recalled 2,408 Flexible Cryoprobes (REF 20402-411) used in surgery nationwide, including Puerto Rico. Probes may rupture or burst during activation. Hospitals and healthcare providers should stop using the device and follow recall instructions. Manufacturer contact will provide remediation.

Erbe USA
Probes
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Endoscope Reprocessor OER-Elite Recall Affects 2,929 Units (2026)

Olympus Corporation of the Americas is recalling 2,929 units of the OER-Elite Endoscope Reprocessor in the United States. The MAJ-1443 and MAJ-1444 modules are no longer reprocessing compatible with the OER-Pro and OER-Elite systems. Hospitals and healthcare providers should stop using the affected devices immediately and follow the recall instructions issued by Olympus.

Olympus Corporation of the Americas
The MAJ-1443
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Health & Personal Care
HIGH
FDA DEVICE

Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)

Olympus Corporation of the Americas recalled 3,354 units of the OER-Pro endoscope reprocessor on February 12, 2026. MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

Olympus Corporation of the Americas recalls 47,383 MAJ-1443 and MAJ-1444 endoscope suction valves distributed nationwide in the United States. The valves are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the valves immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Health & Personal Care
HIGH
FDA DEVICE

Erbe USA Recall 33,390 Flexible Cryoprobes Over Rupture Risk (2026)

Erbe USA recalled 33,390 Flexible Cryoprobes with oversheath used in surgery. The devices were distributed nationwide, including Puerto Rico. Probes may rupture during activation. Clinicians should stop using the device immediately and follow recall instructions.

Erbe USA
Probes
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Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-1444 Endoscope Air/Water Valve Recall 2026 for 89,579 Units

Olympus Corporation of the Americas is recalling 89,579 MAJ-1444 endoscope air/water valves distributed nationwide in the United States. The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Healthcare facilities should stop using the devices immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Health & Personal Care
HIGH
FDA DRUG

Eptifibatide Injection Recalled Over Labeling Error

Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.

EPTIFIBATIDE
Labeling: Not
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Health & Personal Care
HIGH
FDA DEVICE

CareFusion 303 BD Alaris System with Guardrails Suite MX Recall Impacts 1,025,567 Units (2026)

CareFusion 303 recalled 1,025,567 units of the BD Alaris System with Guardrails Suite MX with Point of Care Unit worldwide. The recall concerns labeling that fails to indicate which TLS version must be enabled for secure hospital Wi-Fi communication. Hospitals and clinicians should stop using the device immediately and follow manufacturer instructions. The recall was issued by the FDA and is being

CareFusion 303
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.

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

Waldemar Link Embrace Shoulder Drill Tower Recalled After Mislabeling; 75 Units in 2026

Waldemar Link GmbH & Co. KG recalled 75 Embrace Shoulder Drill Tower devices distributed to U.S. hospitals after discovering mixed-up article numbers in the device overview. The surgical steps are correct, but the overview labeling is inaccurate. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions sent by email.

Waldemar Link GmbH & Co. KG
The surgical
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Category Statistics

Total Recalls
1,620
Pages
81