stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
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.
Frederik's by Meijer Focaccia Bread Recalled for Metal Fragments (2026)
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Palmetto Gourmet Foods Vegetarian Chicken Flavor Ramen Recalled for Yellow #5 (5,664,960 Units, 2026
Palmetto Gourmet Foods Recalls 12.9M Vegetarian Chicken Flavor Ramen Express 3oz for Undeclared Red/
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.
Bader Enterprises Premium Food Bubble Gum Recalled for 400 lbs Undeclared Blue Colors (2026)
Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Bader Enterprises Recalls Premium Food Jordan Almonds in 2.0 oz & 3.5 oz Packaging (2026 Recall)
Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
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.
Olympus Insufflation Unit Recalled Over Software Malfunction
Issue with software algorithm which may lead to overpressure events.
Olympus Insufflation Unit Recalled Due to Software Hazard
Issue with software algorithm which may lead to overpressure events.
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.
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 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.