International safety notice
Cánula de perfusión aórtica EZ Glide™ de Edwards Lifesciences, modelos EZC21A, EZC21TA, EZC24A, EZC24TA, EZF21A, EZF21TA, EZF24A, EZF24TA, EZS21A, EZS21TA, EZS24A y EZS24TA
Spain / AEMPS · ESP · Nov 28, 2019
Key facts
| Title | Cánula de perfusión aórtica EZ Glide™ de Edwards Lifesciences, modelos EZC21A, EZC21TA, EZC24A, EZC24TA, EZF21A, EZF21TA, EZF24A, EZF24TA, EZS21A, EZS21TA, EZS24A y EZS24TA |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Cánula de perfusión aórtica EZ Glide™ de Edwards Lifesciences, modelos EZC21A, EZC21TA, EZC24A, EZC24TA, EZF21A, EZF21TA, EZF24A, EZF24TA, EZS21A, EZS21TA, EZS24A y EZS24TA |
| Manufacturer | Edwards Lifesciences LLC, EEUU |
| Models | EZF21TA, 206768, 207324, EZF21A, 229054, 214216, 206772, 226938, 227494, 206369, 46980, 220151 and 118 more |
| Event type | Safety Notice |
| Date | Nov 28, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1