Transmotion Medical Recall

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Class 2 Device Recall TransMotion Stretcher Chair

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=148797

Class 2 Device Recall TransMotion Stretcher Chair. TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving,...

Recall of Device Recall Transmotion Medical TMM5

https://medicaldevices.icij.org/events/usa-device-recall-transmotion-medical-tmm5

TransMotion Medical Inc. sent an Urgent Medical Device Recall letter dated November 4, 2014, to all affected customers. The letter identified the product the problem and the …

Class 2 Device Recall Transmotion Medical TMM5

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=131309

TransMotion Medical Inc. sent an Urgent Medical Device Recall letter dated November 4, 2014, to all affected customers. The letter identified the product the …

Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls

The FDA posts summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that …

Medical Device Recalls

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=21&event_id=&productdescriptiontxt=utp&productcode=&rootCauseText=¢erclassificationtypetext=&recallnumber=&postdatefrom=&postdateto=&productshortreasontxt=&firmlegalnam=&PMA_510K_Num=&pnumber=&knumber=&sortcolumn=pdd

FDA Recall Posting Date. Recalling Firm. TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair. Intended use is to provide the... 2 10/10/2016 Winco Mfg., LLC …

TRANSMOTION TMM SERIES TROUBLESHOOTING …

https://www.manualslib.com/manual/1514390/Transmotion-Tmm-Series.html

Summary of Contents for Transmotion TMM Series. Page 1 Introduction This troubleshooting guide references devices manufactured during different time …

MAUDE Adverse Event Report: TRANSMOTION …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=4457734

Transmotion medical inc designed a new pendant which was released in 05/2013. The new pendant s considerably more durable than the older style pendants. The new …

GE HealthCare Recalls Nuclear Medicine 600/800 Series …

https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

See Medical Device Recall Database entry for more information. Distribution Dates: April 1, 2018 to December 16, 2022; Devices Recalled in the U.S.: 688; Date Initiated by Firm: December 18, 2022;

MAUDE Adverse Event Report: TRANSMOTION …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=4417561

The new pendant has been in production for 17 months and there have been no reports of the new pendant cause the device to move on its own. Additionally, in 11/2014, …

TransMotion Collection - Champion.

https://www.championchair.com/transmotion/

TransMotion Collection. Innovative seating built to optimize patient flow from admission thru discharge, all on a single surface. The TransMotion Collection can help minimize …

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Class 2 Device Recall TransMotion Stretcher Chair

Recall of Device Recall Transmotion Medical TMM5

Class 2 Device Recall Transmotion Medical TMM5

Medical Device Recalls | FDA

Medical Device Recalls

TRANSMOTION TMM SERIES TROUBLESHOOTING …

MAUDE Adverse Event Report: TRANSMOTION …

GE HealthCare Recalls Nuclear Medicine 600/800 Series …

MAUDE Adverse Event Report: TRANSMOTION …

TransMotion Collection - Champion.

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