MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-09-17 for 3612 LITE GLOVE 31140257 manufactured by Covidien.
[55335166]
An investigation is currently underway. Upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10
[55335167]
It was reported to covidien on (b)(6) 2016 that a customer had an issue with a lite glove. The customer reports that when pulling over onto the covidien handle, the gloves tear apart. There was no patient present.
Patient Sequence No: 1, Text Type: D, B5
[55486350]
Submit date: 09/17/2016.
Patient Sequence No: 1, Text Type: N, H10
[55486351]
The customer stated that the lite glove was too tight when placing on the handle and then split as a result. The split was found when placing on the handle during setup and a new glove was placed. A medtronic handle was being used with the lite glove.
Patient Sequence No: 1, Text Type: D, B5
[62835325]
Investigation summary: the investigation determined that the issue is most likely caused by process variability and dimensional tolerance that may lead to rare incidences of the light glove splitting upon application to the devon? Light handle adapter. The dimensional tolerance issue was related to a slight reduction of the inside diameter of the handle cover. This reduction in diameter was implemented to eliminate pleats in the glove and minimize the potential for splits and tears. Corrective actions: a capa was initiated, a root cause was determined, and corrective action taken. Process modifications were made to address the dimensional tolerance and reduce difficulty during application, while maintaining a design that is free of pleats. This modification has already been implemented. To mitigate further occurrences, additional process improvements were implemented and include updates to both equipment and inspection criteria. As an additional mitigation step, the product labeling has been updated instructing the user to inspect the light glove for barrier integrity after application to the light handle. Along with this labeling update, medtronic initiated a field safety notification in october 2016 notifying our customers of labeling update. Although the product met specifications and acceptable production quality limits medtronic recognized the opportunity to further reduce risk by conducting the fsn and updating the instructions for use.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 9612030-2016-00436 |
| MDR Report Key | 5958943 |
| Date Received | 2016-09-17 |
| Date of Report | 2016-09-15 |
| Date Mfgr Received | 2016-12-16 |
| Device Manufacturer Date | 2016-02-02 |
| Date Added to Maude | 2016-09-17 |
| 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 | EDWARD ALMEIDA |
| Manufacturer Street | 15 HAMPSHIRE STREET |
| Manufacturer City | MANSFIELD MA 02048 |
| Manufacturer Country | US |
| Manufacturer Postal | 02048 |
| Manufacturer Phone | 5084524151 |
| Manufacturer G1 | COVIDIEN |
| Manufacturer Street | CALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL |
| Manufacturer City | TIJUANA |
| Manufacturer Country | MX |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | 3612 LITE GLOVE |
| Generic Name | LITE GLOVE |
| Product Code | LYU |
| Date Received | 2016-09-17 |
| Model Number | 31140257 |
| Catalog Number | 31140257 |
| Lot Number | 60277100564X |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Manufacturer Address | CALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL TIJUANA MX |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-09-17 |