MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other,user facility report with the FDA on 2020-02-18 for BD POSIFLUSH? SF SALINE SYRINGE 306499 manufactured by Bd Medical (bd West) Medical Surgical.
[188257967]
Investigation summary: no samples or photos were received; therefore, sample analysis could not be performed and the condition reported by the customer could not be confirmed. Complaints received for this device and reported condition will continue to be tracked and trended. Information will be captured on trend reports and monitored monthly. Our business team regularly reviews the collected data for identification of emerging trends. A device history record review was completed with zero defects found. No quality notifications were written for this batch, nor for the associated assembly batches. Investigation conclusion: unconfirmed: bd was not able to duplicate or confirm the customer? S indicated failure as no samples or photos were returned. This is the 1st complaint for lot # 9018598 for this type of defect or symptom. There was no documentation for this type of defect during the entire production run of this batch. Root cause description: it was recommended to ask the customer to verify their system. It could be that this catalog # was uploaded with the incorrect description. Rationale: capa not required at this time.
Patient Sequence No: 1, Text Type: N, H10
[188257968]
It was reported that the bd posiflush? Sf saline syringe barcode scanned as "heparin" instead of "normal saline" before use. The following information was provided by the initial reporter: "it was reported the product is scanning as heparin but the catalog states the product is normal saline. Verbatim: upon scanning, we received a warning stating the barcode does not match the appropriate product. "
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1911916-2020-00166 |
| MDR Report Key | 9723255 |
| Report Source | OTHER,USER FACILITY |
| Date Received | 2020-02-18 |
| Date of Report | 2020-02-05 |
| Date of Event | 2020-02-03 |
| Date Mfgr Received | 2020-02-04 |
| Device Manufacturer Date | 2019-01-18 |
| Date Added to Maude | 2020-02-18 |
| 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 | BDX BRETT WILKO |
| Manufacturer Street | 9450 SOUTH STATE STREET |
| Manufacturer City | SANDY UT 84070 |
| Manufacturer Country | US |
| Manufacturer Postal | 84070 |
| Manufacturer Phone | 8015652341 |
| Manufacturer G1 | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
| Manufacturer Street | 1852 10TH AVENUE |
| Manufacturer City | COLUMBUS NE 68601 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 68601 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BD POSIFLUSH? SF SALINE SYRINGE |
| Generic Name | INTRAVASCULAR CATHETER |
| Product Code | NGT |
| Date Received | 2020-02-18 |
| Catalog Number | 306499 |
| Lot Number | 9018598 |
| Device Availability | * |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
| Manufacturer Address | 1852 10TH AVENUE COLUMBUS NE 68601 US 68601 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2020-02-18 |