DISPOSABLE BANANA BLADE HPS-BLD

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01,07,08 report with the FDA on 2013-05-03 for DISPOSABLE BANANA BLADE HPS-BLD manufactured by Conmed Linvatec.

Event Text Entries

[3165510] The customer reported that during use of the hsp-bld (disposable banana blade) in a hip arthroscopy on a (b)(6), female patient, the tip of the blade broke off inside the joint and could not be found/removed. The surgeon opted to complete the procedure with a plan for a post-operative surgery to locate and remove the broken tip at a later time. Subsequently, a second surgery was performed one week later on (b)(6) 2013 and the tip was successfully removed at that time. Follow-up with the user facility revealed that the user reused this "single use" disposable banana blade. Name and address of the reprocessor was not provided. Latest follow-up with the customer indicated that there are no side effects or infections on the patient's hip and she is doing fine at the present time.
Patient Sequence No: 1, Text Type: D, B5


[10687829] To date the device has not been returned from the user facility for evaluation. A follow up report will be filed upon receipt of the device and completion of the evaluation. Device has not yet been returned.
Patient Sequence No: 1, Text Type: N, H10


[10847040] Conmed linvatec received the broken blade in two distinct pieces for evaluation. Visual inspection of the returned disposable banana blade confirmed the reported breakage and found the blade was separated from the shaft. Micrograph examination revealed the broken blade exhibited some amount of wear to the cutting surface (nicks) and the wear was considered to be consistent with a product that had been used several times. Further evaluation found the shaft handle presented with rust-like areas scattered across the handle surface. Micrograph analysis in the area of separation between the blade and shaft handle revealed a fractured metal break without significant distortion to the geometry of the two pieces. A localized area of dense discoloration and rust-like appearance that remained in the cross-section of the fracture was noted. This suggests that the blade had been cracked or partially separated, allowing chemicals to intrude into the partial break. Once trapped these could contribute localized rusting leading to a clean break at a later time under far less stress. All of these factors strongly indicate that this single-use product has been used more than one time. A review of the device history records showed lot #391348 was manufactured on august 20, 2012 in a lot of (b)(4) units with no noted discrepancies during the manufacturing process that could have caused or contributed to the reported breakage. In addition, there were no other similar complaints received for this item and lot number combination. This product is intended to cut soft, thick tissue during hip arthroscopy. This failure mode is addressed in the risk document as an acceptable risk. A letter of education regarding this type of breakage along with the evaluation results will be forwarded to the customer.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1017294-2013-00016
MDR Report Key3092278
Report Source00,01,07,08
Date Received2013-05-03
Date of Report2013-04-08
Date of Event2013-04-04
Date Mfgr Received2013-04-08
Device Manufacturer Date2013-08-20
Date Added to Maude2013-05-03
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. BRENDA JOHNSON
Manufacturer Street11311 CONCEPT BLVD.
Manufacturer CityLARGO FL 33773
Manufacturer CountryUS
Manufacturer Postal33773
Manufacturer Phone7273995515
Manufacturer G1CONMED LINVATEC
Manufacturer Street11311 CONCEPT BLVD.
Manufacturer CityLARGO FL 33773
Manufacturer CountryUS
Manufacturer Postal Code33773
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDISPOSABLE BANANA BLADE
Generic NameKNIFE, ORTHOPEDIC
Product CodeHTS
Date Received2013-05-03
Returned To Mfg2013-05-10
Catalog NumberHPS-BLD
Lot Number391348
Device Expiration Date2017-08-19
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCONMED LINVATEC
Manufacturer Address11311 CONCEPT BLVD. LARGO FL 33773 US 33773


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2013-05-03

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