Product Safety Recalls

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Bovie Medical Corporation Recall 87274

Description: ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

Bovie Medical Corporation Recall 87274 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1155-2021
Event ID87274
Event DescriptionConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
Product TypeDevices
DistributionUS Nationwide distribution in the states of CA and FL.
Quantity5270 units
Recall ReasonThere can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.
Device Classification20210310
Device Code InfoCatalog Numbers C3390A (lots 0317F, 0417B, 0517B, 0517D, 0517J, 0617D, 0617F, 0617H, 0617K, 0717A, 0717G, 0817B, 0917G, 0917J, 1017C, 1017E, 1017J, 1117B, 0418C); C3350A (lots 0317F, 0417B, 0517B, 0517G, 0717C, 0817D, 0917C, 0917E); C3350NA (lots 0317F, 0517G, 0817F); C2455NA (lots 0317F, 0517B, 0717E, 1017C, 1017E); C1860NA (lots 0317F, 0517B, 0717E, 0817F, 1017G, 0418E); C3390NA (lots 0317F, 0517G, 0817H, 1017J, 0418E, 0518F, 1218C).
Center Classification Date20210226
Recall Initiation Date20210201
Recalling FirmBovie Medical Corporation
Initial Notification E-Mail
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