Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identified a
FDA device recall Z-1512-2017 · posted 2017-03-08 · Terminated
Recall details
- Recalling firm
- Devicor Medical Products Inc
- 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.
- 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.
- Root cause
- Process control
- Status
- Terminated
- Product code
- KNW
- Quantity affected
- 320
- Distribution
- Worldwide Distribution - US including IA, IL, NY, OH, OK, PA, TN & WV. Internationally to Chile and Brazil
- Date initiated
- 2017-02-28
- Date posted
- 2017-03-08
- Date terminated
- 2017-08-03
- Location
- Cincinnati, OH
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| Mammotome revolve Dual Vacuum Assist Biopsy System (K152989) | Devicor Medical Products, Inc. | 2016-02-25 |