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calendar

13,661 catalysts · 3,350 8k filing · 2,401 grant · 2,188 approval · 1,517 device 510k · 1,123 device recall · 1,026 device pma

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  • 8k filing3,350
  • grant2,401
  • approval2,188
  • device 510k1,517
  • device recall1,123
  • device pma1,026
device adverse event
1,000
  • earnings584
  • recall391
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    • Oncology148
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    Week of Oct 27, 2025

    50
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    Burette Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. BURETTE SET W/ 2 CARESITE, 134 IN.; Catalog Number: 490159. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog numbers: 1. EXTENSION SET, 18 IN; Catalog Number: 490448. 2. EXTENSION SET, 52 IN.; Catalog Number: 490465. 3. EXTENSION SET 49 IN.; Catalog Number: 490486. 4. EXTENSION SET, 12 CARESTITE LADS; Catalog Number: 490577. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/ 15DROPS/ML; Catalog Number: 490508. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    Blood Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. Y-TYPE BLOOD SET, HAND PUMP, 146 IN.; Catalog Number: 490438. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    SafeDAY set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET 60 DROP W/2 SAFEDAY; Catalog Number: 352635. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV SET W/2 CARESITE & 2 ULTRAPORT ZERO; ULTRAPORT Zer0 IV Set with CARESITE; Catalog Number: 457504. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET, 2 CARESITES, 125 IN.; Catalog Number: 490408. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/15 DR / mL W/ EXT SET; Catalog Number: 490208. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET, 15DR, CARESITE LAD, 130 IN; Catalog Number: 477002. 2. IV ADMIN SET 85 IN.; Catalog Number: 477017. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/15 DROPS/ML, 128 IN.; Catalog Number: 480231. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    B.BRAUN utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/ 60 DROPS/ML,141 in.; Catalog Number: 490349. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET W/15 DROPS/ML, 134 IN.; Catalog Number: 490477. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    Extension Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. ET08US EXTENSION SET W/ULTRA Y SITE; Catalog Number: 474912. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV SET 15DR 5CARESITE 1 ULRAPORT, 141 IN; Catalog Number: 490067. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. IV ADMIN SET,2 CARESITE, TRIP MANIFOLD; Catalog Number: 490343. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 29, 2025device recall291d agoB Braun Medical Inc device recall (Cls II)B. Braun Medical Inc

    Outlook set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.; Catalog Number: 490564. — Reason: Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025approval290d agoTYRUKO (NATALIZUMAB-SZTN) — FDA approvalnatalizumab biosimilar

    Sponsor: SANDOZ INC. Form: INJECTABLE. Route: INJECTION

    full page →natalizumab biosimilar →fda approvals ↗
    ›Oct 30, 2025approval290d agoVIMIZIM (ELOSULFASE ALFA) — FDA approvalBIOMARIN PHARMACEUTICAL INC

    Sponsor: BIOMARIN PHARM. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 30, 2025approval290d agoHALDOL (HALOPERIDOL DECANOATE) — FDA approvalJanssen Therapeutics

    Sponsor: JANSSEN PHARMS. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 30, 2025approval290d agoAXITINIB — FDA approvalaxitinib SR

    Sponsor: APOTEX. Form: TABLET. Route: ORAL

    full page →axitinib SR →fda approvals ↗
    ›Oct 30, 2025approval290d agoEVEROLIMUS — FDA approvalPostsurgical Therapeutics Inc

    Sponsor: NOVUGEN. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 30, 2025device 510k290d agoTornier, Inc. — Tornier Humeral Reconstruction System Max (Tornier HRS Max) (510k cleared)

    Product code: KWT. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoShenzhen Kaiyan Medical Equipment Co., Ltd. — Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1) (510k cleared)

    Product code: OAP. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoDetax GmbH — Freeprint® denture flex (510k cleared)

    Product code: EBI. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoImperative Care, Inc. — Zoom System (Zoom 4S Catheter) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoCarefusion (Bd) — BD Alaris Pump Infusion Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoArctx Medical — Arctx Cool Catheter Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoHangzhou AllTest Biotech Co., Ltd. — AllTest Urinary Tract Infection Test (510k cleared)Hangzhou DAC Biotech Co Ltd

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoDiasorin Molecular, LLC — Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoTaewoong Medical Co., Ltd. — Niti-S Esophageal Stent; Esophageal TTS Stent (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoMerchsource, LLC — AIR COMPRESSION BOOTS 1018195,1018196 (510k cleared)

    Product code: IRP. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoBoston Scientific Corporation — OBSIDIO™ Conformable Embolic (M0013972101010) (510k cleared)BOSTON SCIENTIFIC CORP

    Product code: KRD. Advisory committee: Cardiovascular. Type: Special

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoParagon Implant Mfg., LLC — GEN5 and GEN5+ Dental Implant System (510k cleared)

    Product code: DZE. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoCytrellis Biosystems, Inc. — ellacor System with Micro-Coring Technology (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoViTAA Medical Solutions, Inc. — AiORTA - Plan (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoM.I.Tech Co., Ltd. — HANAROSTENT Esophagus Upper (CCC) (510k cleared)YSX Tech Co., Ltd

    Product code: ESW. Advisory committee: General, Plastic Surgery. Type: Special

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k290d agoBoston Scientific Corporation — Moses™ 200 D/F/L Laser Fiber (M0068130100); Moses™ 365 D/F/L Laser Fiber (M0068130110); Moses™ 550 D/F/L Laser Fiber (M0068130120) (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device pma290d agoMedtronic, Inc. — SYNERGYST II PULSE GENERATOR MODELS 7070 & 7071 (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoSiemens Medical Solutions Diagnostics Limited — IMMULITE 2000 Free PSA (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTG. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoABBOTT MEDICAL — TactiFlex™ Ablation Catheter, Sensor Enabled ™ (TactiFlex SE) (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoMedtronic, Inc. — Avalus Bioprosthesis (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoGuardant Health, Inc. — Shield (PMA supplement)Guardant Health, Inc.

    Supplement type: 30-Day Notice. Product code: PHP. Advisory committee: MG. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoMedtronic, Inc. — OmniaSecure™ MRI SureScan™ Lead Model 3930M (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoSiemens Healthcare Diagnostics, Inc. — IMMULITE 2000 AFP (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LOK. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoABBOTT MEDICAL — Epic™, Epic™ Supra, Epic™ Plus, Epic™ Plus Supra and Epic™ Max Stented Tissue Valve (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma290d agoSiemens Healthcare Diagnostics, Inc. — IMMULITE 2000 PSA (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTF. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device recall290d agoCepheid device recall (Cls II)

    Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10 — Reason: Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall290d agoOlympus Corporation of the Americas device recall (Cls I)

    Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Number: HX-400U-30 Used with an Olympus endoscope to deliver a nylon loop snare. — Reason: Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall290d agoCepheid device recall (Cls II)

    Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10 — Reason: Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall290d agoInpeco S.A. device recall (Cls II)

    FlexLab (FLX); Version: FLX-217-40; — Reason: The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes — Status: Ongoing

    full page →fda device recalls ↗
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    $YSXT
    $BSX51.83+0.27%
    $BSX51.83+0.27%
    $MDT91.27+0.76%
    $BMRN67.36-1.71%
    $MDT91.27+0.76%
    $GH131.78+2.07%
    $MDT91.27+0.76%