These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 10335996)

  • 1. Blood component recalls in the United States.
    Ramsey G; Sherman LA
    Transfusion; 1999 May; 39(5):473-8. PubMed ID: 10335996
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Managing recalls and withdrawals of blood components.
    Ramsey G
    Transfus Med Rev; 2004 Jan; 18(1):36-45. PubMed ID: 14689376
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Blood product recalls in the United States.
    McCullough J; Riley E; Lindgren B; Pulkrabek S; Hall R; Riley W
    Transfusion; 2014 Sep; 54(9):2276-82. PubMed ID: 24863173
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Blood component recalls and market withdrawals: frequency, reasons, and management in the United States.
    Ramsey G
    Transfus Med Rev; 2013 Apr; 27(2):82-90. PubMed ID: 23375736
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Software-Related Recalls of Health Information Technology and Other Medical Devices: Implications for FDA Regulation of Digital Health.
    Ronquillo JG; Zuckerman DM
    Milbank Q; 2017 Sep; 95(3):535-553. PubMed ID: 28895231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Blood component recalls in the United States, 1998.
    Ramsey G; Sherman LA
    Transfusion; 2000 Feb; 40(2):253-4. PubMed ID: 10686012
    [No Abstract]   [Full Text] [Related]  

  • 7. Characteristics of FDA drug recalls: A 30-month analysis.
    Hall K; Stewart T; Chang J; Freeman MK
    Am J Health Syst Pharm; 2016 Feb; 73(4):235-40. PubMed ID: 26843501
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Research: Evaluation of Orthopedic Hip Device Recalls by the FDA from 2007 to 2017.
    Peters W; Pellerin C; Janney C
    Biomed Instrum Technol; 2020 Nov; 54(6):418-426. PubMed ID: 33339030
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The nature and pattern of coronary stent recalls.
    Kumar S; Innasimuthu AL; Marmur JD
    J Invasive Cardiol; 2014 Sep; 26(9):433-6. PubMed ID: 25198486
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Medical device recalls and the FDA approval process.
    Zuckerman DM; Brown P; Nissen SE
    Arch Intern Med; 2011 Jun; 171(11):1006-11. PubMed ID: 21321283
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Use of Recalled Devices in New Device Authorizations Under the US Food and Drug Administration's 510(k) Pathway and Risk of Subsequent Recalls.
    Kadakia KT; Dhruva SS; Caraballo C; Ross JS; Krumholz HM
    JAMA; 2023 Jan; 329(2):136-143. PubMed ID: 36625810
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Blood component recalls.
    Bozzo T
    Transfusion; 1999 May; 39(5):439-41. PubMed ID: 10335990
    [No Abstract]   [Full Text] [Related]  

  • 13. A cross-sectional study of prevalence, distribution, cause, and impact of blood product recalls in the United States.
    Alqemlas I; Shankar S; Handagama W; Felse PA
    Blood Adv; 2020 Apr; 4(8):1780-1791. PubMed ID: 32343797
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Major FDA medical device recalls in ophthalmology from 2003 to 2015.
    Talati RK; Gupta AS; Xu S; Ghobadi CW
    Can J Ophthalmol; 2018 Apr; 53(2):98-103. PubMed ID: 29631834
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Current good manufacturing practices for blood and blood components: notification of consignees receiving blood and blood components at increased risk for transmitting HIV infection--FDA. Final rule.
    Fed Regist; 1996 Sep; 61(175):47413-23. PubMed ID: 10160337
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Overview of high-risk medical device recalls in obstetrics and gynecology from 2002 through 2016: implications for device safety.
    Janetos TM; Ghobadi CW; Xu S; Walter JR
    Am J Obstet Gynecol; 2017 Jul; 217(1):42-46.e1. PubMed ID: 28500861
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Twenty-Two Years of U.S. Meat and Poultry Product Recalls: Implications for Food Safety and Food Waste.
    Gorton A; Stasiewicz MJ
    J Food Prot; 2017 Apr; 80(4):674-684. PubMed ID: 28294687
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Medical Device Recalls in Orthopedics: Recent Trends and Areas for Improvement.
    Vajapey SP; Li M
    J Arthroplasty; 2020 Aug; 35(8):2259-2266. PubMed ID: 32279947
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Overview of Class I Device Recalls in Diagnostic Radiology, 2002-2015.
    Ghobadi CW; Hayman EL; Xu S
    J Am Coll Radiol; 2016 Jun; 13(6):638-43. PubMed ID: 26922597
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An exploratory analysis of U.S. FDA Class I medical device recalls: 2014-2018.
    Sarkissian A
    J Med Eng Technol; 2018 Nov; 42(8):595-603. PubMed ID: 30896310
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.