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Class 2 Device Recall Invacare PerfectO2 V Oxygen …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=184169
- Recall Status 1: Open 3, Classified: Recall Number: Z-0514-2021: Recall Event ID: 86604: 510(K)Number: K200890 Product Classification: Generator, oxygen, portable - Product Code CAW: Product:...
Invacare Corporation - Product Recall
- http://www.invacare.com/cgi-bin/imhqprd/inv_productalert/prod_alert.jsp?s=0
- Product Recall URGENT MEDICAL DEVICE FIELD ACTIONInvacare® Perfecto2V Oxygen Concentrator (Model Numbers: IRC5PO2V and IRC5PO2VC) Involving stationary oxygen …
Class 3 Device Recall Invacare Platinum 5NXG Oxygen …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=193498
- Invacare Corporation 877-413-6008 Manufacturer Reason for Recall: Between March 2, 2021 and December 31, 2021, the product label used in production …
Class 2 Device Recall Invacare 9805 and 9805P …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=167386
- Invacare Corporation 1200 Taylor St Elyria OH 44035-6248: For Additional Information Contact: Customer Service 877-413-6008 Manufacturer Reason for Recall: …
Class 2 Device Recall Invacare - Food and Drug …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=190405
- Letter states reason for recall, health risk and action to take: Visit www. Invacare.com/RC916 within five (5) business days of receiving this notice. Enter the …
Product Recall - Invacare Corporation
- https://dealer.invacare.com/productRecall
- INVACARE WORLDWIDE Product Recall URGENT MEDICAL DEVICE FIELD ACTION - Invacare Hydraulic Patient Lift (Model Number 9805 and 9805P) The letter is to provide …
Invacare to restructure financially, two subsidiaries file Chapter 11
- https://www.massdevice.com/invacare-financial-restructuring-subsidiaries-chapter-11/
- Invacare said it filed a number of customary “first-day” motions for court approval. This helps to facilitate a smooth transition into Chapter 11 and support …
Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
- If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. …
Invacare Corporation - Medical Device Recall Home
- http://www.invacare.com/cgi-bin/imhqprd/genericContentTemplate2.jsp?sideButton=generic&sideButCatEdName=Medical+Device+Recall+Side+Button+Categories&catOID=-536891934&searchable=false&sortBy=pri
- Invacare Corporation is the world's leading manufacturer of wheelchairs, respiratory products and other home health care and mobility products for people with disabilities. …
Product Recalls | Invacare
- https://www.invacare.com.au/support/product-recalls
- Invacare has learned that the PSI (Pressure Sensitive Interrupter) design for the compressor motor start/run capacitor by one supplier could lead to rupture. That capacitor in the …
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