Product Safety Recalls

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Covidien, LLC Recall 91318

Description: COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1

Covidien, LLC Recall 91318 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0955-2023
Event ID91318
Event DescriptionCOVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Product TypeDevices
DistributionForeign Distribution: Hong Kong
Quantity21 units
Recall ReasonThe product is labeled with the incorrect expiration date.
Device Classification20230118
Device Code InfoUDI/DI (GTIN): 10884521825765, Lot Number: 520200
Center Classification Date20230112
Recall Initiation Date20221123
Recalling FirmCovidien, LLC
Initial Notification Visit
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