MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-10-26 for AFFIRM? VPIII AMBIENT TEMPERATURE TRANSPORT SYSTEM 446255 manufactured by Bd Infusion Therapy Systems Inc. S.a. De C.v..
[58456608]
Affirm vpiii ambient temperature transport system is a sterile ready-to-use system intended for the collection, transport and preservation of vaginal specimens for use only with the affirm vpiii microbial identification test. The affirm vpiii ambient temperature transport system (atts) should be used with those specimens where transport times are expected to exceed 1 h at ambient temperature (15? 30? C) or 4 h at refrigerated temperatures (2? 8? C). Bd molecular quality initiated investigation on a customer complaint for an affirm atts injury (finger puncture) during specimen processing due to glass in the specimen processing tube. It was confirmed that the end user found glass in the specimen collection tube. Quality investigation required review of the affirm atts package insert and affirm collection poster. Per review of the affirm package insert and collection poster, it was determined that the affirm collection site was not following the affirm atts package insert or affirm collection poster instructions. The collection site was crushing the atts glass ampoule (as instructed), opening the atts cap and pouring the glass into the affirm sample collection tube (not instructed). The affirm package insert and affirm collection poster does not instruct collection sites to open the atts vial and pour the glass into the collection tube. Bd will update the affirm collection poster to provide further clarification on the instructions of use with affirm atts. Bd molecular quality will continue to closely monitor for trends associated with affirm atts glass injury. (b)(4). Device not returned to manufacturer.
Patient Sequence No: 1, Text Type: N, H10
[58456609]
The customer reported that while processing a patient specimen transport tube from a affirm vpiii ambient temperature transport system, glass pierced through the tube and injured a technician's thumb. The technician reported the incident and received basic first aid and care according to the facility's blood borne pathogens policy. Bd followed up with the customer on october 17, 2016 and the injured technician is reported to be doing well.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9610847-2016-00040 |
MDR Report Key | 6058923 |
Date Received | 2016-10-26 |
Date of Report | 2016-10-26 |
Date of Event | 2016-10-05 |
Date Mfgr Received | 2016-10-07 |
Date Added to Maude | 2016-10-26 |
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 | MEDICAL TECHNOLOGIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | BDX CAROL NIETO |
Manufacturer Street | 7 LOVETON CIRCLE |
Manufacturer City | SPARKS MD 21152 |
Manufacturer Country | US |
Manufacturer Postal | 21152 |
Manufacturer Phone | 4103164000 |
Manufacturer G1 | BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. |
Manufacturer Street | PERIFERICO LUIS DONALDO COLOSIO NO. 579 |
Manufacturer City | NOGALES |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | AFFIRM? VPIII AMBIENT TEMPERATURE TRANSPORT SYSTEM |
Generic Name | DEVICE, SPECIMEN COLLECTION |
Product Code | LIO |
Date Received | 2016-10-26 |
Catalog Number | 446255 |
Lot Number | UNKNOWN |
Operator | MEDICAL TECHNOLOGIST |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. |
Manufacturer Address | PERIFERICO LUIS DONALDO COLOSIO NO. 579 NOGALES US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2016-10-26 |