stop use immediately Recalls

2,229 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DRUG

Med Nap Cleansing Towelettes Recall Expanded Over CGMP Deviations (2026)

ACME United Corporation recalls Med Nap Cleansing Towelettes, 5"x7" Benzalkonium Chloride 0.13%, distributed nationwide. CGMP Deviations prompted the recall. Stop using the product now and contact ACME United or a healthcare provider for guidance.

MED NAP CLEANSING TOWELETTE
CGMP Deviations
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Overpressure Hazard

Olympus Corporation recalled 744 High Flow Insufflation Units on January 16, 2026. A software algorithm issue may lead to overpressure events during use. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DRUG

Specialty Process Labs Issues Recall for Subpotent Thyroid Drug

Specialty Process Labs recalled 58 grams of Thyroid, USP due to subpotency. The recall affects products distributed nationwide. Consumers should stop using the drug immediately and contact their healthcare provider.

Specialty Process Labs
Subpotent Drug
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Health & Personal Care
HIGH
FDA DEVICE

CVS Wound Care Device Recalled Due to Sterile Barrier Breach

CVS recalled 2,906 units of its wound care device on January 16, 2026. The recall stems from potential packaging failures that may compromise sterility. Affected products include model number CVS405406, distributed across multiple states and internationally.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalls Shoulder Prosthesis Over Labeling Error

Encore Medical, LP recalled 20 shoulder prosthesis implants on January 15, 2026. Incorrect labeling on the RSP Standard Humeral Socket Insert poses a high hazard risk. Affected products were distributed nationwide across multiple states.

Encore Medical, LP
Knee and
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Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalled Humeral Socket Insert Over Labeling Issues

Encore Medical, LP recalled 20 units of its RSP Humeral Socket Insert on January 15, 2026. The recall stems from incorrect labeling on knee and humeral socket implants. Patients and healthcare providers should stop using the device immediately.

Encore Medical, LP
Knee and
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    stop use immediately Recalls | RecallRadar