PLASTIC LIP AND CHEEK SELF-RETAINING RETRACTOR, SELF RETAINING, CHILD SIZE N/A 09-0136

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-01-30 for PLASTIC LIP AND CHEEK SELF-RETAINING RETRACTOR, SELF RETAINING, CHILD SIZE N/A 09-0136 manufactured by Biomet Microfixation.

Event Text Entries

[98849361] (b)(4). Device product code: eig. (b)(4). Customer has indicated that the product is in process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[98849362] It was reported eight packages for child-sized lip retractors contained lip retractors that were too large. This was identified upon receipt. No patient involvement. No adverse events have been reported as a result of the malfunction.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001032347-2018-00052
MDR Report Key7228189
Date Received2018-01-30
Date of Report2018-05-18
Date Mfgr Received2018-04-21
Device Manufacturer Date2017-08-09
Date Added to Maude2018-01-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. MICHELLE COLE
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal32218
Manufacturer Phone9047414400
Manufacturer G1BIOMET MICROFIXATION
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal Code32218
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePLASTIC LIP AND CHEEK SELF-RETAINING RETRACTOR, SELF RETAINING, CHILD SIZE
Generic NameRETRACTOR; DENTAL HAND INSTRUMENT
Product CodeEIG
Date Received2018-01-30
Model NumberN/A
Catalog Number09-0136
Lot Number100025169
ID NumberSEE H10 NARRATIVE
OperatorOTHER HEALTH CARE PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET MICROFIXATION
Manufacturer Address1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218


Patients

Patient NumberTreatmentOutcomeDate
10 2018-01-30

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