fda
10 records
FDA Device Recall: Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Softwa
2024-06-12
Class II — Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.
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FDA Recall: Verathon, Inc. — Class III
20210811
Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality. | Product: GlideScope Go Monitors
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FDA Device Recall: GlideScope Go Monitors
2021-08-11
Class III — Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.
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FDA Device Recall: GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideS
2020-07-15
Class I — When video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or excessive torsion to the connection port, this force is transferred to the HDMI P...
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FDA Device Recall: GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
2020-03-18
Class II — A typographical error in the Operations & Maintenance Manual incorrectly identifies the use of low level disinfection for the reusable video laryngoscope, specifically for the Titanium Blad...
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FDA Device Recall: It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg).
2017-04-26
Class II — Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged with the incorrect size device (GVL 1 Stat (blades)).
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FDA Device Recall: BladderScan BVI 9600, Model Numbers: 0270-0451, 0270-0452, 0270-0754, and U270-0
2016-03-16
Class II — The firm is providing customers with an updated Operations and Maintenance Manual for each of the BladderScan BVI 9600 and AortaScan AMI 9700 devices. The updated Operations and Maintenanc...
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FDA Device Recall: GlideScope AVL Video Laryngoscope (AVL), Part Number AVL 3- 0574-0115; AVL 4-057
2015-12-23
Class II — Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blades may separate, due to inadequate bonding of the silicone adhesive affixing the halves of the blade. The potent...
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FDA Device Recall: GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5
2013-06-26
Class I — Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to the potential risk of premature failure/breakage of the blade tip that may not be readily visible during routine ins...
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FDA Device Recall: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporate
2012-12-19
Class I — Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5 were recalled due to potential cracking.
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nppes
1 records
USASpending
1 records
Federal Award: VERATHON INC — $1,274,486
2026-04-01
EXPRESS REPORT: NX ORDERS PLACED FOR THE MONTH OF APRIL 2026
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