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calendar

88 catalysts · 37 grant · 21 device 510k · 11 device recall · 10 device pma · 9 approval

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2026-08-10: 0 catalysts2026-08-11: 16 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: 20 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 8 catalysts2026-11-03: 17 catalysts2026-11-04: 22 catalysts2026-11-05: 36 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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no tagged catalysts yet

Week of Feb 2, 2026

50
›Feb 6, 2026approval186d agoANAGRELIDE HYDROCHLORIDE — FDA approvalTakeda Pharmaceuticals USA Inc

Sponsor: BARR LABS. Form: CAPSULE. Route: ORAL

full page →fda approvals ↗
›Feb 6, 2026approval186d agoOLANZAPINE AND FLUOXETINE HYDROCHLORIDE (FLUOXETINE HYDROCHLORIDE) — FDA approvalFLUOXETINE HYDROCHLORIDE

Sponsor: EPIC PHARMA LLC. Form: CAPSULE. Route: ORAL

full page →FLUOXETINE HYDROCHLORIDE →fda approvals ↗
›Feb 6, 2026approval186d agoGLYCOPYRROLATE — FDA approvalFresenius Kabi USA LLC

Sponsor: PH HEALTH. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Feb 6, 2026approval186d agoIDARUBICIN HYDROCHLORIDE — FDA approvalIDARUBICIN HYDROCHLORIDE

Sponsor: PFIZER. Form: SOLUTION. Route: INTRAVENOUS

full page →IDARUBICIN HYDROCHLORIDE →fda approvals ↗
›Feb 6, 2026approval186d agoPRAVASTATIN SODIUM — FDA approvalSenores Pharmaceuticals Inc

Sponsor: SENORES PHARMS. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Feb 6, 2026approval186d agoTICAGRELOR — FDA approvalTICAGRELOR

Sponsor: MANKIND PHARMA. Form: TABLET. Route: ORAL

full page →TICAGRELOR →fda approvals ↗
›Feb 6, 2026approval186d agoNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalNOREPINEPHRINE BITARTRATE

Sponsor: BAXTER HLTHCARE CORP. Form: SOLUTION. Route: INTRAVENOUS

full page →NOREPINEPHRINE BITARTRATE →fda approvals ↗
›Feb 6, 2026approval186d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

full page →DOXYCYCLINE HYCLATE →fda approvals ↗
›Feb 6, 2026approval186d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

Sponsor: STRIDES PHARMA INTL. Form: TABLET. Route: ORAL

full page →DOXYCYCLINE HYCLATE →fda approvals ↗
›Feb 6, 2026device 510k186d agoAthelas, Inc. — Athelas Home (510k cleared)

Product code: GKZ. Advisory committee: Hematology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoK2m, Inc. — Q Interbody Instruments (510k cleared)

Product code: OLO. Advisory committee: Neurology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoQuantel Medical — INTEGRE LIO (510k cleared)

Product code: HQF. Advisory committee: Ophthalmic. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoEieling Technology (Shenzhen) Limited — Liver fat ultrasound quantitative system, The FattaLab (FL-CC M1, FL-CC M1_Pro) (510k cleared)

Product code: IYO. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoGe Medical Systems, LLC — SIGNA™ Bolt (510k cleared)

Product code: LNH. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoSiemens Healthcare Diagnostics, Inc. — Atellica® IM TSH3-Ultra II (TSH3ULII) (510k cleared)

Product code: JLW. Advisory committee: Clinical Chemistry. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoStryker Leibinger GmbH & Co KG — Spine Guidance 5.3 Software; Q Interbody Instruments; Elite Q Attachments; Elite Cutting Accessories (510k cleared)

Product code: OLO. Advisory committee: Neurology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoUzinmedicare Co., Ltd. — Spectra S1 Pro; Spectra S2 Pro (510k cleared)

Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoLive Medica, LLC — LiveMedica Enterprise PACS (510k cleared)

Product code: LLZ. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoFujifilm Corporation — Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood DH-134STR (510k cleared)Fujifilm Holdings Corp

Product code: FDS. Advisory committee: Gastroenterology, Urology. Type: Special

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoSafeBeat Rx, Inc. — SafeBeat Rx App (510k cleared)

Product code: DQK. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoMedian Technologies — Median LCS (internal name) / eyonis LCS (trade name) (1.0) (510k cleared)

Product code: QDQ. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoPhilips Medizin Systeme Boeblingen GmbH — IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) (510k cleared)

Product code: MHX. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoShenzhen Gsd Technology Co., Ltd. — Dermatrix Duo (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

Product code: GEI. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoKneevoice, Inc. — Kneevoice Cartilage Evaluation System (750-3600-001) (510k cleared)

Product code: DQD. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoDentsply Sirona, Inc. — Stainless Steel Surgical Kits (510k cleared)DENTSPLY SIRONA Inc.

Product code: KCT. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoETHICON, Inc. — MONOCRYL™ Plus Antibacterial Poliglecaprone – 25 (Monofilament), Sterile Synthetic Absorbable Surgical Suture (510k cleared)

Product code: GAM. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoInova Diagnostics, Inc. — Aptiva APS IgA Reagent (510k cleared)Co-Diagnostics, Inc.

Product code: MSV. Advisory committee: Immunology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoAmferia AB — Amferia Wound Dressing (510k cleared)

Product code: SHA. Advisory committee: General, Plastic Surgery. Type: Direct

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoAugmented Reality Software S.L. — LAIA XR (510k cleared)

Product code: LLZ. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device 510k186d agoBalmoral Medical, LLC — ROSA Knee System with UltraSound Imaging Platform (USIP) (510k cleared)

Product code: OLO. Advisory committee: Neurology. Type: Traditional

full page →fda device 510k ↗
›Feb 6, 2026device pma186d agoEdwards Lifesciences, LLC — TRIFORMIS RESILIA Tricuspid Valve, Model 11300T (PMA supplement)Edwards Lifesciences Corp

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

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoEdwards Lifesciences, LLC — TRIFORMIS RESILIA Tricuspid Valve, Model 11300T (PMA supplement)Edwards Lifesciences Corp

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

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoMedtronic Neuromodulation — Altaviva™ Tibial Neuromodulation System (Altaviva™ P7850N) (PMA supplement)

Supplement type: 30-Day Notice. Product code: QPT. Advisory committee: GU. Decision: OK30

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoAbiomed, Inc. — Impella 2.5 System; Impella CP System; Impella CP with Smart Assist System; Impella 5.0 System, Impella 5.5 with Smart A (PMA supplement)Abion Inc

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

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoSpectranetics Corp. — ELCA Coronary Atherectomy Catheters (PMA supplement)

Supplement type: 135 Review Track For 30-Day Notice. Product code: LPC. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoMedtronic, Inc. — SynchroMed™ Infusion System, Ascenda™ Intrathecal Catheters (Drug Delivery Infusion Pump 8667) (PMA supplement)Medtronic plc

Supplement type: 30-Day Notice. Product code: LKK. Advisory committee: HO. Decision: OK30

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoMedtronic, Inc. — Activa™ Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™ (DBS, DBS Neurostimulator Implantable, DBS Neuros (PMA supplement)Medtronic plc

Supplement type: 30-Day Notice. Product code: MHY. Advisory committee: NE. Decision: OK30

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoMedtronic Neuromodulation — Master Restore™, Itrel™, Synergy Intellis™, Vanta™ and Inceptiv™ Spinal Cord Stimulation Systems and Pisces™, Specify™, (PMA supplement)

Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoInspire Medical Systems — INSPIRE II UPPER AIRWAY STIMULATOR (PMA supplement)Inspire Medical Systems, Inc.

Supplement type: Normal 180 Day Track. Product code: MNQ. Advisory committee: AN. Decision: APPR

full page →fda device pma ↗
›Feb 6, 2026device pma186d agoAbiomed, Inc. — Impella RP System, Impella RP with Smart Assist System, Impella RP Flex System (PMA supplement)Abion Inc

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

full page →fda device pma ↗
›Feb 6, 2026device recall186d agoTrividia Health, Inc. device recall (Cls I)HENRY SCHEIN INC

Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE METRIX PRO Meter Only/RE4099P-40, Henry Schein TRUE METRIX PRO Kit/RE4099P-43, McKESSON TRUE METRIX PRO Meter Only/RE4051P-00, Moore Medical TRUE METRIX PRO Meter Only/RE4068P-01. — Reason: The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoInternational Life Sciences device recall (Cls II)

Artelon FlexBand Dynamic Matrix Ref: 31057 — Reason: Augmentation devices failed bacterial endotoxin testing. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoTrividia Health, Inc. device recall (Cls I)

Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR Kit/REA4011-01, Meijer TRUE METRIX AIR Kit/REA4019-01, Publix TRUE METRIX AIR Kit/REA4020-01, Discount Drug Mart TRUE METRIX AIR Kit/REA4025-01, HEB TRUE METRIX AIR Kit/REA4031-01, SunmarkTRUE METRIX AIR Kit/REA4054-01, Rite AidTRUE METRIX AIR Kit/REA4066-01, Centerwell TRUE METRIX AIR Kit/REA4081-01, HumanaTRUE METRIX AIR Meter Only/REA4081-40, Centerwell TRUE METRIX AIR Starter Kit/REA4081-43, Healthmart TRUE METRIX AIR Kit/REA4089-01, Relion TRUE METRIX AIR Kit/REA4094-01, Relion TRUE METRIX AIR Kit/REA4094-01RX, Kroger TRUE METRIX AIR Kit/REA4203-01, Foster and Thrive TRUE METRIX AIR Kit/REA4211-01, TRUE METRIX AIR Kit/REA4H01-01, TRUE METRIX AIR NFRS Meter Only/REA4H01-40, TRUE METRIX AIR NFRS Starter Kit/REA4H01-43, TRUE METRIX AIR Kit (mg/dL)/REA4i03-01, TRUE METRIX AIR Starter Kit (mg/dL)/REA4i03-02, Walmart (MediMart) TRUE METRIX AIR Meter Only (Mexico - mg/dL)/REA4i04-00, TRUE METRIX AIR Kit (Australia - mmol/L)/REA4i81-11, TRUE METRIX AIR Kit (United Kingdom - mmol/L)/REA4i82-11, TRUE METRIX AIR Starter Kit (United Kingdom - mmol/L)/REA4i82-12 — Reason: The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose. — Status: Ongoing

›Feb 6, 2026device recall186d agoBD KIESTRA LAB AUTOMATION device recall (Cls II)

BD Kiestra" ReadA; Catalog No.: 446948. — Reason: In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred, there was potential for delays in plate retrieval from the incubator while connectivity was restored. This issue was intermittent and did not affect test results, performance of the assay, or sample integrity. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoDatascope Corp. device recall (Cls III)

Battery Charging Station; Model: 0998-00-0802; — Reason: The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoTrividia Health, Inc. device recall (Cls I)

Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX GO Kit/RF4001-01BK, CVS TRUE METRIX GO Kit/RF4007-01, Meijer TRUE METRIX GO Kit/RF4019-01, Fred's Phamarcy TRUE METRIX GO Kit/RF4023-01, HEB TRUE METRIX GO Kit/RF4031-01, Hyvee TRUE METRIX GO Kit/RF4048-01, Rite Aid TRUE METRIX GO Kit/RF4066-01, TopCo TRUE METRIX GO Kit/RF4209-01, TRUE METRIX GO Kit/RF4H01-01BK, TRUE METRIX GO NFRS Meter Only/RF4H01-40, TRUE METRIX GO Kit (Jamaica - mmol/L)/RF4i29-11BK, TRUE METRIX GO Kit (Australia - mmol/L)/RF4i81-11BK, TRUE METRIX GO Kit (United Kingdom - mmol/L)/RF4i82-11BK, TRUE METRIX GO Starter Kit (United Kingdom - mmol/L)/RF4i82-12BK — Reason: The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoHitachi, Ltd. Radiation Oncology Systems, Kashiwanoha device recall (Cls II)

Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR — Reason: Software anomaly in the patient positioning system may result in positional discrepancy. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoInternational Life Sciences device recall (Cls II)

Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1) — Reason: Augmentation devices failed bacterial endotoxin testing. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoInternational Life Sciences device recall (Cls II)

Artelon FlexBand Plus Ref: 41054 & 41057 — Reason: Augmentation devices failed bacterial endotoxin testing. — Status: Ongoing

full page →fda device recalls ↗
›Feb 6, 2026device recall186d agoTrividia Health, Inc. device recall (Cls I)HENRY SCHEIN INC

Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX Kit/RE4001-01, Leader TRUE METRIX Kit/RE4002-01, Leader TRUE METRIX Meter Only/RE4002-40, CVS TRUE METRIX Kit/RE4007-01SB, GNP TRUE METRIX Meter Only/RE4011-00, GNP TRUE METRIX Kit /RE4011-01, MEIJER TRUE METRIX Kit/RE4019-01, FRED'S TRUE METRIX Kit/RE4023-01, DISCOUNT DRUG TRUE METRIX Kit/RE4025-01, KINRAY TRUE METRIX Kit/RE4027-01, HEB TRUE METRIX Kit/RE4031-01, McKesson TRUE METRIX Starter Kit/RE4051-43, SUNMARK TRUE METRIX Meter Only/RE4054-00, SUNMARK TRUE METRIX Kit/RE4054-01, Signature Care TRUE METRIX Kit/RE4060-01, CareOne TRUE METRIX Kit/RE4061-01, RITE AID TRUE METRIX Kit/RE4066-01, Liberty TRUE METRIX Meter Only/RE4078-40, HUMANA TRUE METRIX Starter Kit/RE4081-03, Wegmans TRUE METRIX Kit/RE4087-01, HEALTHMART TRUE METRIX Meter Only/RE4089-00, HEALTHMART TRUE METRIX Kit/RE4089-01, ARRIVA TRUE METRIX Meter Only/RE4095-40, HealthyAccents TRUE METRIX Kit/RE4097-01, Shopko TRUE METRIX Kit/RE4098-01, Henry Schein TRUE METRIX Kit/RE4099-40, Henry Schein TRUE METRIX Meter Only/RE4099-45, Millennium Pharmay Services TRUE METRIX Kit/RE4202-43, Kroger TRUE METRIX Kit/RE4203-01, TOPCARE TRUE METRIX Kit/RE4209-01, Foster and Thrive TRUE METRIX Kit/RE4211-01, TRUE METRIX Meter Only/RE4H01-00, TRUE METRIX Kit/RE4H01-01, TRUE METRIX Starter Kit/RE4H01-04, TRUE METRIX NFRS Meter Only/RE4H01-40, TRUE METRIX NFRS Starter Kit/RE4H01-43, TRUE METRIX Kit/RE4H01-51, TRUE METRIX Meter Only (mg/dL)/RE4i01-00, TRUE METRIX Kit (mg/dL)/RE4i01-01, TRUE METRIX Kit (mg/dL)/RE4i01-02, TRUE METRIX Starter Kit (mg/dL)/RE4i03-02, TRUE METRIX Kit (mmol/L)/RE4i03-11, Farmacia Benavides TRUE METRIX Meter Only (Mexico - mg/dL)/RE4i05-00, Farmacia del Ahorro TRUE METRIX Meter Only (Mexico - mg/dL)/RE4i07-00, TRUE METRIX Meter Only (Mexico - mg/dL)/RE4i23-00, TRUE METRIX Meter Only (Jamaica - mmol/L)/RE4i29-11, TRUE METRIX Kit (mg/dL)/RE4i61-02, TRUE METRIX Kit (mg/dL)/RE4i61-02THI, TRUE METRIX Kit (United Kingdom - mmol/L)/RE4i82-11, TRUE METRIX Starter Kit (United Kingdom - mmol/L)/RE4i82-12. — Reason: The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose. — Status: Ongoing

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full page →fda device recalls ↗
full page →fda device recalls ↗
$MDT89.41+2.58%
$MDT89.41+2.58%
$XRAY11.66-3.80%
$INSP42.44+0.38%
$CODX1.51000.00%
$FRTRY
$HSIC72.44-2.60%
$EW91.33-2.47%
$PFE27.05+1.08%
$EW91.33-2.47%
$HSIC72.44-2.60%