Calendar

Week of Feb 16, 2026

Feb 18, 2026device recall177d agoHologic, Inc. device recall (Cls II)

Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No — Reason: Due to product exhibiting potential to generate either invalid or false negative results. — Status: Ongoing

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Feb 18, 2026device recall177d agoNavajo Manufacturing Company device recall (Cls I)

Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd — Reason: If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property. — Status: Ongoing

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Feb 18, 2026device recall177d agoMentor Texas, LP. device recall (Cls II)

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc — Reason: Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. — Status: Ongoing

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Feb 18, 2026device recall177d agoMentor Texas, LP. device recall (Cls II)

Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc — Reason: Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. — Status: Ongoing

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Feb 18, 2026device recall177d agoBaxter Healthcare Corporation device recall (Cls I)Baxter Healthcare Corp

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system. — Reason: Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use. — Status: Ongoing

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Feb 18, 2026device recall177d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit per package — Reason: Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals. — Status: Ongoing

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Feb 18, 2026device recall177d agoMedline Industries, LP device recall (Cls II)

Sterile Radiology Procedure Kits, Model Number DYNDH1491B — Reason: There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility. — Status: Ongoing

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Feb 18, 2026grant177d agoBAYLOR COLLEGE OF MEDICINE — Defining the molecular mechanisms driving transovarial transmission of Acari-...Baylor College of Medicine

AI grant. $797,087. PI: Job E Lopez

Week of Feb 16, 2026