TRUCOLOR WRIGHT STAIN 7547177

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07,08 report with the FDA on 2011-09-23 for TRUCOLOR WRIGHT STAIN 7547177 manufactured by Beckman Coulter, Inc..

Event Text Entries

[2261868] A beckman coulter, inc. (bci) employee reported three cases of trucolor wright stain solution leaking from their packages. The events occurred in two separate dates while the employee was packing the cases and involved two different lot numbers. The potential for chemical exposure with the reported incident was present. At one of the events the bci employee reported when lifting the case in the shipping area its content leaked from the box and fell on the clothing. The employee used the emergency shower and was sent home to change clothing. The operator was not wearing personal protection equipment. There was no report of exposure to mucous membranes or open skin lesions. The material safety data sheet (msds) was reviewed and the lab's exposure control or risk mgmt plans are in place. No injuries occurred and medical attention was not sought as a result of this event. No reports of death or serious injury, and no affect to operator safety as a result of this event. This event represents event 1 of 2 events reported by this customer and product quantity of (1).
Patient Sequence No: 1, Text Type: D, B5


[9309674] Per labeling, beckman coulter, inc. Urges its customers to comply with all national health and safety standards such as the use of barrier protection. This may include, but it is not limited to, protective eyewear, gloves, and suitable lab attire when operating or maintaining this or any other automated lab analyzer. Found damaged container/leak from original equipment mfr (oem) vendor during pick and pack process. Based on available info, the root cause can be attributed to product packing was damaged on arrival, causing the reagent to leak. This reportable event was identified during a retrospective review conducted between (b)(4) 2008 and (b)(4) 2010 of complaints for additional reportable events. This mdr represents 1 of 2 reported by this customer. This mdr is related to the following mdr that have been reported: mdr 1061932-2011-01501.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1061932-2011-01500
MDR Report Key2276809
Report Source06,07,08
Date Received2011-09-23
Date of Report2009-03-12
Date of Event2009-02-25
Date Mfgr Received2009-03-12
Device Manufacturer Date2009-01-01
Date Added to Maude2012-06-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMS NORA ZEROUNIAN
Manufacturer Street250 S. KRAEMER BLVD.
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal92821
Manufacturer Phone7149613634
Manufacturer G1BECKMAN COULTER, INC.
Manufacturer Street11800 SW 147TH AVE.
Manufacturer CityMIAMI FL 33196
Manufacturer CountryUS
Manufacturer Postal Code33196
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRUCOLOR WRIGHT STAIN
Product CodeKQC
Date Received2011-09-23
Model NumberNA
Catalog Number7547177
Lot Number9020
ID NumberNA
Device Expiration Date2010-01-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER, INC.
Manufacturer Address11800 SW 147TH AVE. MIAMI FL 33196 US 33196


Patients

Patient NumberTreatmentOutcomeDate
10 2011-09-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.