J-Plasma Precise(R), Catalog Numbers: BVX-150B, BVX-150N, BVX-330B, BVX- 330N, BVX-450B, BVX-450N
FDA Recall Z-1154-2018 · Posted None
Recalling FirmBovie Medical Corporation
Recall StatusTerminated
Product CodeGEI
Date Initiated2018-02-08
Date Terminated2020-09-17
Product Quantity6906 units
Reason for Recall
Bovie Medical is issuing a correction to address incomplete insertion of the J-Plasma(R) handpiece cable plug into the generator receptacle resulting in an incomplete helium seal. The potential exists for patient fluid backflow into the handpiece and the generator receptacle leading to risk of cross-contamination if the generator is reused.
Firm Action
The firm initiated their recall on 02/08/2108 by email to distributors, and letter to the remaining consignees.
Distributors were directed as follows:
"We ask that you immediately:
1. Quarantine your inventory of the J-Plasma Handpieces
o Provide us with a list of catalog numbers and quatities that you have on your possession using the attached Inventory List template.
o Email the information to me at [email protected]
Note: as soon as we receive the information from you we will ship the box labels and insert stuffer notices for the stock that you have on your possession.
o After receiving these labels, please follow the attached instructions on how to add each of the insert stuffer notice and the outer box label to each of the boxes that you have on your possession.
o Document the number of labels/stuffers added to each of the products on the Inventory List provided, sign and date to confirm this was performed.
o Return the signed document to me via email at [email protected].
2. Inform your customers about the correction:
o Identify and contact your customers that have received the product affected by this correction.
o Provide them with a copy of the Urgent Medical Device Correction Template attached to this letter.
o Track and document the customer responses to ensure 100% effectiveness.
o Provide us a summary of the effectiveness of this correction (number of customers impacted and number of responses received)."
The remaining consignees (users of the device) were instructed as follows:
"ACTIONS:
At the end of each procedure, inspect the handpiece cable plug and generator receptacle for the presence of fluids. If fluids are present, immediately discontinue use of the generator.
In addition to following the J-Plasma handpiece Instructions for Use, immediately begin to follow the supplemental instructions provided below to ensure that the J-Plasma handpiece cable plug is properly and co
Root Cause
Nonconforming Material/Component
Distribution Pattern
worldwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.