UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-08-13 for UNK manufactured by .

Event Text Entries

[21609354] Beginning in 2008, and over the last two weeks, we have discovered faulty packaging for a number of different kingli acupuncture needles, compromising sterility and creating a potential hazard for practioners. Although the initial discovery was restricted to packages that contained 5 acupuncture needles. We have subsequently found the same issue with a few single needle kingli packages, as well as with another mfr - acutek. We also found two different instances where it appears that a strand of hair was sealed in the "sterile" kingli package. The principle issue found is that in many instances, the tips of the needles have penetrated the plastic retaining sheath, and protrude from the package compromising both sterility, and creating the needle stick hazard. We have found multiple examples of faulty packaging in both 1" and 1. 5" length needles of various gauges. We took pictures of samples and have retained some of the faulty packages. We also notified our distributer of the problem on 7/24/2008. Please note that this was discovered during the normal course of business, and not as a result of an adverse event. Specifically, with the kingli products, the following 5 needle boxes contained faulty packaging: 1" 32 gauge. 25 x. 25, dated 6/27/2007 to 6/27/2010; 1" 32 gauge. 22 x. 25, dated 11/26/2007 to 11/26/2010; 1" 32 gauge. 20 x. 25, dated 9/25/07 to 9/25/2010; 1. 5" 30 gauge. 30x 40 dated 10/7/2005 to 10/7/2008. 1. 5" 30 gauge. 25 x. 40 dated 10/5/2006 to 10/5/2009. 1. 5" 30 gauge. 20 x. 40 dated 9/25/2007 to 9/25/2010. Should add'l info be required please contact us.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5007986
MDR Report Key1113983
Date Received2008-08-13
Date of Report2008-08-12
Date of Event2008-07-21
Date Added to Maude2008-08-22
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameUNK
Generic NameKINGLI ACUPUNCTURE NEEDLES
Product CodeMQX
Date Received2008-08-13
Device AvailabilityY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key1120357


Patients

Patient NumberTreatmentOutcomeDate
10 2008-08-13

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