Similar articles for PMID: 22021778

Year	Number of Results
1869	1
1871	1
1978	1
1989	1
1991	1
1993	2
1996	2
1997	1
2001	1
2003	1
2004	1
2005	3
2006	2
2008	1
2009	2
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2011	3
2012	3
2013	2
2014	6
2015	6
2016	7
2017	12
2018	8
2019	4
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2022	3
2023	3
2024	0

1

Medical-device recalls in the UK and the device-regulation process: retrospective review of safety notices and alerts.

Heneghan C, Thompson M, Billingsley M, Cohen D. Heneghan C, et al. BMJ Open. 2011 May 15;1(1):e000155. doi: 10.1136/bmjopen-2011-000155. BMJ Open. 2011. PMID: 22021778 Free PMC article.

2

MEDICAL DEVICE RECALLS IN CANADA FROM 2005 TO 2015.

Gagliardi AR, Takata J, Ducey A, Lehoux P, Ross S, Trbovich PL, Easty A, Bell CM, Urbach DR. Gagliardi AR, et al. Int J Technol Assess Health Care. 2017 Jan;33(6):708-714. doi: 10.1017/S0266462317000824. Epub 2017 Sep 18. Int J Technol Assess Health Care. 2017. PMID: 28918758

3

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. Janetos TM, et al. Am J Obstet Gynecol. 2017 Jul;217(1):42-46.e1. doi: 10.1016/j.ajog.2017.03.021. Epub 2017 May 10. Am J Obstet Gynecol. 2017. PMID: 28500861

4

Ronquillo JG, Zuckerman DM. Ronquillo JG, et al. Milbank Q. 2017 Sep;95(3):535-553. doi: 10.1111/1468-0009.12278. Milbank Q. 2017. PMID: 28895231 Free PMC article.

5

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. Kadakia KT, et al. JAMA. 2023 Jan 10;329(2):136-143. doi: 10.1001/jama.2022.23279. JAMA. 2023. PMID: 36625810 Free PMC article.

6

Comparison of rates of safety issues and reporting of trial outcomes for medical devices approved in the European Union and United States: cohort study.

Hwang TJ, Sokolov E, Franklin JM, Kesselheim AS. Hwang TJ, et al. BMJ. 2016 Jun 28;353:i3323. doi: 10.1136/bmj.i3323. BMJ. 2016. PMID: 27352914 Free PMC article.

7

Analysis of Medical Device Alerts Issued by the Portuguese Medicines Agency: Scoping the Purpose of New Regulatory Recommendations.

Pires C, Duarte D, Cavaco A. Pires C, et al. Acta Med Port. 2021 Mar 1;34(3):201-208. doi: 10.20344/amp.13419. Epub 2021 Mar 1. Acta Med Port. 2021. PMID: 33971115 Free article.

8

Assessment of cardiovascular and noncardiovascular medical device recalls.

Somberg JC, McEwen P, Molnar J. Somberg JC, et al. Am J Cardiol. 2014 Jun 1;113(11):1899-903. doi: 10.1016/j.amjcard.2014.03.024. Epub 2014 Mar 17. Am J Cardiol. 2014. PMID: 24837271

9

Recalls and safety alerts involving pacemakers and implantable cardioverter-defibrillator generators.

Maisel WH, Sweeney MO, Stevenson WG, Ellison KE, Epstein LM. Maisel WH, et al. JAMA. 2001 Aug 15;286(7):793-9. doi: 10.1001/jama.286.7.793. JAMA. 2001. PMID: 11497532

10

Recalls and safety alerts affecting automated external defibrillators.

Shah JS, Maisel WH. Shah JS, et al. JAMA. 2006 Aug 9;296(6):655-60. doi: 10.1001/jama.296.6.655. JAMA. 2006. PMID: 16896108

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