MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-22 for A-SPOT 651 manufactured by Beekley Corporation.
[124658703]
The customer notified beekley of the product issue on (b)(6) 2018. However, the customer confirmed that a patient had their mammogram repeated due to the product issue on (b)(6) 2018.
Patient Sequence No: 1, Text Type: N, H10
[124658704]
The imaging component of the a-spot palpable mass marker separated from the adhesive component and therefore did not show up on the mammogram image. As a result, the mammogram was repeated.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9021987-2018-00005 |
| MDR Report Key | 7992331 |
| Date Received | 2018-10-22 |
| Date of Report | 2018-10-22 |
| Date of Event | 2018-09-12 |
| Date Mfgr Received | 2018-10-08 |
| Device Manufacturer Date | 2016-06-15 |
| Date Added to Maude | 2018-10-22 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | KATE CHASE |
| Manufacturer Street | 1 PRESTIGE LANE |
| Manufacturer City | BRISTOL CT 06010 |
| Manufacturer Country | US |
| Manufacturer Postal | 06010 |
| Manufacturer Phone | 8605834700 |
| Manufacturer G1 | BEEKLEY CORPORATION |
| Manufacturer Street | 1 PRESTIGE LANE |
| Manufacturer City | BRISTOL CT 06010 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 06010 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | A-SPOT |
| Generic Name | PALPABLE MASS MARKER |
| Product Code | JAC |
| Date Received | 2018-10-22 |
| Returned To Mfg | 2018-10-08 |
| Model Number | 651 |
| Catalog Number | 651 |
| Lot Number | 651.06151601 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BEEKLEY CORPORATION |
| Manufacturer Address | 1 PRESTIGE LANE BRISTOL CT 06010 US 06010 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-10-22 |