ECHELON 60MM REINFORCEMENT
Report
- Report Number
- 3005075853-2022-02774
- Event Type
- Malfunction
- Date Received
- May 3, 2022
- Date of Event
- April 12, 2022
- Report Date
- May 2, 2022
- Manufacturer
- ETHICON ENDO-SURGERY, LLC.
- Product Code
- OXC
- UDI-DI
- 10705036023296
- PMA / PMN Number
- K190937
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
(B)(4). BATCH #: UNK. A MANUFACTURING RECORD EVALUATION WAS PERFORMED FOR THE FINISHED DEVICE LOT NUMBER, AND NO [NON-CONFORMANCES/ MANUFACTURING IRREGULARITIES] WERE IDENTIFIED. ATTEMPTS HAVE BEEN MADE TO RETRIEVE THE DEVICE. TO DATE THE DEVICE HAS NOT BEEN RETURNED. IF THE DEVICE OR FURTHER DETAILS ARE RECEIVED AT A LATER DATE A SUPPLEMENTAL MEDWATCH WILL BE SENT. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL REPORT, A FOLLOW-UP REPORT WILL BE FILED AS APPROPRIATE.
(B)(4). DATE SENT: 6/2/2022. ADDITIONAL INFORMATION AN ANALYSIS OF THE PRODUCT COULD NOT BE PERFORMED SINCE A PHYSICAL SAMPLE WAS NOT RECEIVED FOR EVALUATION. AS PART OF OUR COMPANY QUALITY SYSTEM PROCESS, ALL DEVICES ARE MANUFACTURED, INSPECTED, AND DISTRIBUTED TO APPROVED SPECIFICATIONS. HOWEVER, IF THE PRODUCT IS RECEIVED AT A LATER DATE, THE INVESTIGATION WILL BE UPDATED AS APPLICABLE.
IT WAS REPORTED THAT THE DEVICES WERE FOUND ON THEIR SHELVES WITH THE INDICATORS BEING PINK. FACILITY STATED THAT THEY HAVE BEEN USING THESE SINCE THE FOURTH OF APRIL AND ARE UNSURE IF ANY OF THE LABELS OF THE DEVICES USED WERE ALSO PINK. NO PATIENT CONSEQUENCES REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2075293 | ECHELON 60MM REINFORCEMENT | OXC | OXC | ETHICON ENDO-SURGERY, LLC. | ECH60R | RBCCMSS0 | 10705036023296 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown |