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.
163 related articles for article (PubMed ID: 10267947)
1. A medical device recall and reporting system. Guideline report. Alder HC Hosp Technol Ser; 1983 Dec; 2(32):1-21. PubMed ID: 10267947 [No Abstract] [Full Text] [Related]
2. Facilities' responsibilities after notification of a medical device hazard or recall. Health Devices; 2004 Sep; 33(9):339. PubMed ID: 15532863 [No Abstract] [Full Text] [Related]
3. Limiting your liability for malfunctioning equipment. Hosp Secur Saf Manage; 1987 Jun; 8(2):5-7. PubMed ID: 10282644 [No Abstract] [Full Text] [Related]
4. Hospitals wary of interpretation of medical device reporting law. Burke M Hospitals; 1991 Oct; 65(20):40, 42. PubMed ID: 1916713 [No Abstract] [Full Text] [Related]
7. Experts see dangers in rules implementing Safe Medical Devices Act. Wagner M Mod Healthc; 1992 Feb; 22(7):36-9. PubMed ID: 10116238 [TBL] [Abstract][Full Text] [Related]
8. Medical devices; various proposed rules for device classification; withdrawal of proposed rules. Food and Drug Administration. Withdrawal of proposed rules. Fed Regist; 1982 Mar; 47(54):11880-2. PubMed ID: 10254383 [TBL] [Abstract][Full Text] [Related]
9. Safe Medical Devices Act: reporting rules face hurdle. Shepherd M; Furst E Health Facil Manage; 1996 Apr; 9(4):38. PubMed ID: 10156096 [No Abstract] [Full Text] [Related]
10. Knowing your equipment: a vital element in risk management. Hyman WA Tex Hosp; 1980 Apr; 35(11):48-9. PubMed ID: 10246497 [No Abstract] [Full Text] [Related]
11. Lessons learned from the Hospital Experience Reporting System. Beck WC; Geffert JP; Comella LH Med Instrum; 1983; 17(5):343-6. PubMed ID: 6646020 [TBL] [Abstract][Full Text] [Related]
12. Medical device reporting regulations. Gill PG Va Med Q; 1997; 124(1):8-12. PubMed ID: 9009849 [No Abstract] [Full Text] [Related]
13. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting. Food and Drug Administration, HHS. Final rule. Fed Regist; 2000 Jan; 65(17):4112-21. PubMed ID: 11010653 [TBL] [Abstract][Full Text] [Related]
14. Challenges in regulating breakthrough medical devices. Muni NI; Gross TP; Boam AB; Wang S; Zuckerman BD Food Drug Law J; 2005; 60(2):137-42. PubMed ID: 16097092 [No Abstract] [Full Text] [Related]
15. Medical device safety: FDA's postmarket transformation initiative. Schultz D Food Drug Law J; 2007; 62(3):593-6. PubMed ID: 17915401 [No Abstract] [Full Text] [Related]
16. New regulation requires reporting of significant medical device problems. FDA Drug Bull; 1984 Dec; 14(3):26. PubMed ID: 6526175 [No Abstract] [Full Text] [Related]
17. What is the Medical Device and Lab Product Problem Reporting Program? Moore R Pharm Times; 1982 Nov; 48(11):53-7. PubMed ID: 10257641 [No Abstract] [Full Text] [Related]
18. Careful with that equipment! Sosin J RN; 2002 Feb; 65(2):59-60, 62. PubMed ID: 15328869 [No Abstract] [Full Text] [Related]