MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-14 for A1603, 6MM L/L STEALTH CLIP 3/4 F 10/BX UNK manufactured by Applied Medical Resources.
[177619167]
No product is being returned for evaluation and no lot # has been provided to manufacturer. A final report will be sent once the results have been analyzed.
Patient Sequence No: 1, Text Type: N, H10
[177619168]
Complaint 1 out of 12 (complaint #(b)(4)). Complaint 2 out of 12 (complaint #(b)(4)). Complaint 3 out of 12 (complaint #(b)(4)). Complaint 4 out of 12 (complaint #(b)(4)). Complaint 5 out of 12 (complaint #(b)(4)). Complaint 6 out of 12 (complaint #(b)(4)). Complaint 7 out of 12 (complaint #(b)(4)). Complaint 8 out of 12 (complaint #(b)(4)). Complaint 9 out of 12 (complaint #(b)(4)). Complaint 10 out of 12 (complaint #(b)(4)). Complaint 11 out of 12 (complaint #(b)(4)). Complaint 12 out of 12 (complaint #(b)(4)). Procedure performed: cabg - coronary artery bypass. "stealth clips (x12) have not been closing once applied to blood vessel. This lack of occlusion has been causing blood vessel to have blood leakage until another stealth clip can be applied. " additional information received via telephone on 31dec2019 from account manager: none of the complaint clips were saved. The rep will request that the client attempt to save the product if this complaint occurs again. The clip complaints was noted over a period of time, however it is currently unclear how long this period of time was. The rep is planning to reach out to the client to determine the number of affected cases, the dates, and the procedures. Additional information received via email on 08jan2020 from account manager: "i [name] spoke with the account contact. Because this has happened over a 3 month period and they just notified on me in december, they do t have the information of dates and specific procedures that the device malfunctioned. " the three month period was clarified to be referring to october 2019 to december 2019. Intervention: another stealth clip applied. Patient status: no patient injury.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2027111-2020-00309 |
| MDR Report Key | 9588979 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2020-01-14 |
| Date of Report | 2020-02-10 |
| Date Mfgr Received | 2019-12-17 |
| Date Added to Maude | 2020-01-14 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | WENDY KOBAYASHI |
| Manufacturer Street | 22872 AVENIDA EMPRESA |
| Manufacturer City | RANCHO SANTA MARGARITA CA 92688 |
| Manufacturer Country | US |
| Manufacturer Postal | 92688 |
| Manufacturer Phone | 9497138059 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | A1603, 6MM L/L STEALTH CLIP 3/4 F 10/BX |
| Generic Name | CLIP, VASCULAR |
| Product Code | DSS |
| Date Received | 2020-01-14 |
| Model Number | A1603 |
| Catalog Number | UNK |
| Lot Number | UNK |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | APPLIED MEDICAL RESOURCES |
| Manufacturer Address | 22872 AVENIDA EMPRESA RANCHO SANTA MARGARITA CA 92688 US 92688 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-01-14 |