Recall Z-1512-2017
Devicor Medical Products Inc · initiated February 28, 2017
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identified as suspicious under imaging guidance
Codes / lots: F11621304D1
Reason for recall
The device did not have Revolve Stereo Probe labeling, no product code indicating the size and length of the probe, no sterilization sticker or lot number.
FDA-determined cause: Process control
Action taken
Devicor sent an Urgent Medical Device Recall letter dated March 10, 2017 to all affected consignees via first class mail. The recall response rate will be tracked and reconciled by consignee's response form, certifications of product inventory, and/or disposal. Consignees were asked to complete and return the enclosed response form as soon as possible. Consignees with any questions were instructed to call Mammotome Customer Service at 1-877-926-2666. For questions regarding this recall call 513-864-9158.
Details
- Recall number
- Z-1512-2017
- Initiated
- February 28, 2017
- Posted by FDA
- March 8, 2017
- Terminated
- August 3, 2017
- Product code
- KNW – Instrument, Biopsy
- Quantity
- 320
- Distribution
- Worldwide Distribution - US including IA, IL, NY, OH, OK, PA, TN & WV. Internationally to Chile and Brazil
- Recalling firm
- Devicor Medical Products Inc, Cincinnati, OH