KY JELLY PERSONAL LUBRICANT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-27 for KY JELLY PERSONAL LUBRICANT manufactured by Reckitt Benckiser Healthcare Int. Limited.

Event Text Entries

[118389909] The consumer agreed to return sample but has not. A sample from the same batch# from which the consumer's product was derived was tested and was found to be within specifications. (b)(6) consent was obtained and release was sent to consumer, but has not been returned to (b)(4) to date. No medical records available.
Patient Sequence No: 1, Text Type: N, H10


[118389990] Kidney infection [kidney infection]. Kidney pain [renal pain]. Patient could not urinate without feeling pain on lower back sides [dysuria]. Case description: report no 1, received date: 04-feb-2016. Received from consumer relations, country: united states, reference no: (b)(4). Suspect product: ky jelly lubrication unspecified. Case reference number us-(b)(6) is a spontaneous case report sent by a consumer which refers to an unknown female patient. It was reported that about 3 months ago on?? -??? -2015 a patient of an unknown age started using ky jelly lubrication unspecified, frequency, route, indication, stop date and duration were all unknown. She said that she had no irritation or discomfort while using the product. A week later on?? -??? -2015 was rushed to the hospital because of a severe kidney infection. She was fine about two weeks after. She started using the product again because she did not see the link between her medical issue and the product. Once again rushed to the hospital with another kidney infection and this time the symptoms were much worst. She then searched for what could have caused this condition, until they talked to a medical professional about the effects of glycerine in the vaginal canal. She was told that the substance found in the product, turns into sugar in the body which could make its way in the urethra and cause severe complications. She reported that she has now stopped using the product and the infection had not re-occurred but felt that her kidneys were damaged permanently, for which they could not urinate without feeling pain on her lower back sides. She continued to suffer at the time of reporting. She also added that she could provide hospital documents on demand. The outcome of the case was not recovered at the time of reporting. Ky jelly lubrication unspecified was dechallenged and the event [? ]kidney infection' was resolved whereas the event [? ]patient could not urinate without feeling pain on lower back sides' persisted. No further information was available at the time of report. Case assessment for ky jelly lubrication unspecified is as follows: the reported serious assessment has not been provided, case relatedness is possible the company's assessment is non serious with a relatedness of possible and unknown. Case outcome: not recovered / not resolved. Report no 2, received date: 11-feb-2016. Received from consumer relations, country: (b)(6), reference no: (b)(6). Information added / updated: country: updated from "united states" to "(b)(4)". Lot number: "a0015c" was added. Age of the patient: "(b)(6) years" was added. Product start date: updated from "?? -??? -2015" to "?? -(b)(6)-2015". Product last date: "(b)(6) 2015" was added. Date of event onset: "(b)(6) 2015" was added. Event: "kidney pain" was added. Qc result "batch investigation was within specifications" was added. Patient stated that she began using ky personal lubricant in (b)(6) of 2015. She said that she had used this product 2-3 times per week. She stated that she had last used this product on (b)(6) 2015. She stated that on (b)(6) 2015, she began to experience severe kidney pains. She stated that she was taken to the hospital via ambulance. She stated that she was admitted to the hospital for 2 days and was diagnosed with a kidney infection. Patient stated that she was treated intravenously with antibiotics, and was sent home with a prescription for oral antibiotics. She stated that although the kidney infection has resolved, she still experiences lower back pain when she urinates. Treatment: iv antibiotics in hospital and oral antibiotics for home. The patient was admitted to hospital, admittance date?? -(b)(6) 2015, discharge date?? -(b)(6) 2015 and 2 days. The case was deemed serious due to hospitalization. No further information was available at the time of report. Follow up has been requested to obtain further information. Case assessment for ky personal lubricant is as follows: the reported serious assessment has not been provided, case relatedness is possible. The reported serious assessment is serious; case relatedness is possible and unlisted. Case outcome: not recovered / not resolved. On (b)(6) 2018: review of historic cases completed by (b)(6) safety physician. Case upgraded to serious and reported. Case comment: diagnosis: kidney infection.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610643-2018-00009
MDR Report Key7820445
Date Received2018-08-27
Date of Report2018-08-27
Date of Event2015-12-25
Date Mfgr Received2016-02-11
Date Added to Maude2018-08-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMS. JOANNE MARTINEZ
Manufacturer StreetDANSOM LANE
Manufacturer CityHULL, HU8 7DS
Manufacturer CountryUK
Manufacturer PostalHU8 7DS
Manufacturer G1RECKITT BENCKISER HEALTHCARE INT. LIMITED
Manufacturer StreetDANSOM LANE
Manufacturer CityHULL, HU8 7DS
Manufacturer CountryUK
Manufacturer Postal CodeHU8 7DS
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameKY JELLY PERSONAL LUBRICANT
Generic NamePERSONAL LUBRICANT
Product CodeNUC
Date Received2018-08-27
Lot NumberA0015C
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerRECKITT BENCKISER HEALTHCARE INT. LIMITED
Manufacturer AddressDANSOM LANE HULL, HU8 7DS UK HU8 7DS


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2018-08-27

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