Verathon, Inc.: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: December 19, 2012. Most recent: June 12, 2024.

Risk classification: Class I: 3 · Class II: 3

Most recent recalls

DateAgencyProduct
June 12, 2024FDABrand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product De…Z-2021-2024
June 12, 2024FDABrand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Versio…Z-2022-2024
July 15, 2020FDAGlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Vide…Z-2476-2020
April 26, 2017FDAIt is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg). Part Num…Z-1852-2017
June 26, 2013FDAGlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable …Z-1558-2013
December 19, 2012FDAThe GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-…Z-0478-2013

Questions about this company

How many recalls does Verathon, Inc. have?
Recalert has 6 U.S. recalls on record for Verathon, Inc., published between December 19, 2012 and June 12, 2024.
What was the most recent Verathon, Inc. recall?
FDA recall Z-2021-2024, published June 12, 2024: Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
Which agencies have handled Verathon, Inc. recalls?
Verathon, Inc. appears as the recalling firm in recalls from: FDA (6).

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