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Smiths Medical ASD Inc. Recall 88741

Description: smiths medical portex Loss of Resistance Device, REF 100/398/000

Smiths Medical ASD Inc. Recall 88741 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0152-2022
Event ID88741
Event Descriptionsmiths medical portex Loss of Resistance Device, REF 100/398/000
Product TypeDevices
DistributionCanada. Belgium, Great Britain, Ireland, Czech Republic, Spain, France, Switzerland, Israel, Germany, Sweden, Italy, New Zealand, Australia, South Africa, Netherlands, Slovenia, United Arab Emirates
Quantity3420 devices
Recall ReasonThe labeling was missing information on sterilization and prohibition of reuse.
Device Classification20211027
Device Code InfoLot Numbers: 3980977, 3986734, 3994302, 3994303 and 4001003
Center Classification Date20211019
Recall Initiation Date20201208
Recalling FirmSmiths Medical ASD Inc.
Initial Notification E-Mail
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