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18,134 catalysts · 4,728 grant · 3,126 8k filing · 2,627 approval · 2,156 device 510k · 1,745 device recall · 1,501 device pma

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2026-08-10: 0 catalysts2026-08-11: 97 catalysts2026-08-12: 19 catalysts2026-08-13: 19 catalysts2026-08-14: 4 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 2 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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  • grant4,728
  • 8k filing3,126
  • approval2,627
  • device 510k2,156
  • device recall1,745
  • device pma1,501
device adverse event
1,000
  • recall586
  • earnings583
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    • Oncology148
    • Infectious Disease46
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    • Pulmonology22
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    Week of Aug 11, 2025

    50
    ›Aug 12, 2025device 510k365d agoLiofilchem — Sulopenem SPM 2 µg (510k cleared)

    Product code: JTN. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 13, 2025recall364d agoBreckenridge Pharmaceutical, Inc. recall (Cls II)Breckenridge Pharmaceutical Inc

    Duloxetine Delayed-Release Capsules, USP, 60mg, 1,000-count bottles, Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-748-10. — Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Lupin Ltd

    Semaglutide +Cyanocobalamin 1.5 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Lupin Ltd

    Semaglutide + Cyanocobalamin injection solution, 2.21 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoDirect Rx recall (Cls II)

    Duloxetine D/R, 20 mg, 30 Caps, 30-count bottle, RX Only, Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037, NDC 61919-422-30 — Reason: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Lupin Ltd

    Semaglutide + Cyanocobalamin 0.88 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 4.4 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Lupin Ltd

    Semaglutide + Cyanocobalamin 0.22 mg + 0.25mg/0.5 ml Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoSUN PHARMACEUTICAL INDUSTRIES INC recall (Cls II)TEVA PHARMACEUTICAL INDUSTRIES LTD

    Spironolactone Tablets, USP, 25 mg, 100-count bottle, Rx only, Mfg. by: Frontida BioPharm, Inc., 1100 Orthodox St, Philadelphia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 53489-143-01 — Reason: Presence of foreign substance: identified as aluminum. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 2.2 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoCardinal Health Inc. recall (Cls II)CARDINAL HEALTH INC

    RECOMBINATE, [Antihemophilic Factor (Recombinant)], 5 mL vials, Rx Only, Takeda Pharmaceuticals USA, Cambridge, MA 02142, NDC: 00944-2843-01 — Reason: CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 11.24 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAlembic Pharmaceuticals Limited recall (Cls II)Alembic Pharmaceuticals Inc

    Doxepin Hydrochloride Capsules, USP, 10 mg, 100 Capsules, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panela v 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-637-31 — Reason: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Lupin Ltd

    Semaglutide + Cyanocobalamin 0.44 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoCardinal Health Inc. recall (Cls II)CARDINAL HEALTH INC

    Xolair (omalizumab injection), 75 mg/0.5 ml, Rx only, Genentech, Inc., South San Francisco, CA 94080, NDC 50242-214-55 — Reason: CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 16.6 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 3 x 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 6.6 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Lupin Ltd

    Semaglutide + Cyanocobalamin 2.67 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 8.8 mg + 1.0mg/0.5 ml Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoCardinal Health Inc. recall (Cls II)CARDINAL HEALTH INC

    Xolair (omalizumab injection), 150 mg/ml, 1 auto-injector, Rx only, Genentech, Inc, South San Francisco, CA 9408, NDC: 50242-215-55. — Reason: CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoAEQUITA PHARMACY recall (Cls II)Eli Lilly and Co

    Tirzepatide + Niacinamide 13.2 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034. — Reason: Lack of Processing Controls. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025recall364d agoDirect Rx recall (Cls II)

    Duloxetine D/R, 30 mg, 30 Caps, RX Only, Packaged as a) 30-count bottle NDC 61919-0482-30, b) 60-count bottle, NDC 61919-0482-60, c) 90-count bottle, NDC 61919-0482-90; Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037, — Reason: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 13, 2025device pma364d agoMedtronic Vascular, Inc. — Protege™ RX Carotid Stent System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NIM. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 13, 2025device pma364d agoAvive Solutions, Inc. — Avive Automated External Defibrillator (AED) System (PMA supplement)Iveda Solutions, Inc.

    Supplement type: Real-Time Process. Product code: MKJ. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 13, 2025device pma364d agoBard Peripheral Vascular, Inc. — FLUENCY PLUS ENDOVASCULAR STENT GRAFT (PMA supplement)

    Supplement type: 30-Day Notice. Product code: PFV. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 13, 2025device pma364d agoEdwards Lifesciences, LLC — Edwards EVOQUE Transcatheter Tricuspid Valve Replacement System (PMA supplement)Edwards Lifesciences Corp

    Supplement type: Normal 180 Day Track No User Fee. Product code: NPW. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 13, 2025device pma364d agoZoll Manufacturing Corporation — LifeVest® Wearable Defibrillator, Model 4000 (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MVK. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 360020-1P — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoBeckman Coulter Inc. device recall (Cls II)

    UniCel DxH 800 COULTER Cellular Analysis System, configured with the Led HGB Photometer REFs:B24802, 629029, B63322 — Reason: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 360020-1EP — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoCHANGE HEALTHCARE CANADA COMPANY device recall (Cls II)

    Change Healthcare Radiology Solutions software version 14.2.2 — Reason: Due to software issue, radiology reports may not be fully displayed when viewing. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243. 3. Brilliance CT Big Bore, Model Number: 728244. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoBeckman Coulter Inc. device recall (Cls II)

    UniCel DxH 900 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C11478 — Reason: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number: 728246. 3. Brilliance CT 6 Slice, Model Number: 728256. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1 — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number: 728231. 3. Ingenuity Flex, Model Number: 728317 — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoBeckman Coulter Inc. device recall (Cls II)

    UniCel DxH 690T COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C34520 — Reason: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 860010-1L — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoBeckman Coulter Inc. device recall (Cls II)

    UniCel DxH 600 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF:B23858 — Reason: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3. Ingenuity CT, Model Number: 728326. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
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