Model Catalog: 3156086 (Lot serial: 121204 to 121499); Model Catalog: 3156075 (Lot serial: 1200101 to 1245680); Model Catalog: 3156076 (Lot serial: 1200101 to 1245680); Model Catalog: 3156084 (Lot serial: 1200101 to 1245680); Model Catalog: 3156085 (Lot serial: 1200101 to 1245680); Model Catalog: 3156086 (Lot serial: 12222407 to 12225241); Model Catalog: 3156085 (Lot serial: 12222407 to 12225241); Model Catalog: 3156084 (Lot serial: 12222407 to 12225241); Model Catalog: 3156076 (Lot serial: 12222407 to 12225241); Model Catalog: 3156075 (Lot serial: 12222407 to 12225241); Model Catalog: 3156074 (Lot serial: 12222407 to 12225241); Model Catalog: 3156074 (Lot serial: 1200101 to 1245680); Model Catalog: 3156085 (Lot serial: 121204 to 121499); Model Catalog: 3156084 (Lot serial: 121204 to 121499); Model Catalog: 3156076 (Lot serial: 121204 to 121499); Model Catalog: 3156075 (Lot serial: 121204 to 121499); Model Catalog: 3156074 (Lot serial: 121204 to 121499); Model Catalog: 3156086 (Lot serial: 1200101 to 1245680
Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.