Health & Personal Care Recalls

ACME United Savannah Antibacterial Towelettes Recalled for CGMP Deviations (2026)

Med-Nap Cleansing Towelettes Recall 2026 for CGMP Deviations

Dynarex Obstetrical Towelettes Cleanser Recall 2026 for CGMP Deviations

ACME United's First Aid Only BZK Towelettes Recall 2026: CGMP Deviations Prompt Nationwide Action

First Aid Only BZK Antiseptic Towelettes Recall for CGMP Deviations (2026)

ACME United Recalls Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes (2026)

Acme United FIRST AID ONLY Hand Sanitizing Wipes Recalled for CGMP Deviations (2026)

Acme United recalled FIRST AID ONLY Hand Sanitizing Wipes, 1,000 wipes per case, nationwide in the United States, on 2026-01-20. The action follows CGMP Deviations cited by the maker. Stop using the wipes and contact Acme United for guidance.

Med Nap Benzalkonium Chloride Antiseptic Towelettes Recall for CGMP Deviations (2026)

Med Nap benzalkonium chloride antiseptic towelettes are recalled for CGMP deviations. They were distributed nationwide by Acme United Corporation. Consumers should stop using the 5x7 inch, 1000-count bulk wipes immediately and contact Acme United for guidance.

ACME UNITED Antimicrobial Hand Wipes Recall 2026 for CGMP Deviations

Dynarex BZK Antiseptic Towelettes 100-Count Recalled for CGMP Deviations (2026)

Green Guard Antiseptic Wipes Recall 2026 Over CGMP Deviations

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.

ACME UNITED Instant Hand Sanitizing Wipes Recalled for CGMP Deviations (2026)

Roche Cobas Pro 1,261-Unit Recall Over Spline-Calibration Error (2026)

Siemens Healthcare Diagnostics Recalls 4,885 Atellica CH Urine Albumin Tests for False Low Results (

Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may report values between 6.2 mg/dL and 40.0 mg/dL.

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.

Integra LifeSciences Recalls Medical Dressing Due to Sterility Risk

Potential packaging failures, which could lead to a breach in the sterile barrier.

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,

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.

Integra LifeSciences Recalls MediHoney Gel for Packaging Issues

Integra LifeSciences Corp. recalled 49,367 units of MediHoney Gel on January 16, 2026. The recall follows potential packaging failures that may compromise the sterile barrier. Affected products include model numbers 31805 and 31815, distributed worldwide.