MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-10-25 for HYTEC 288 PROBE CLEANING SOLUTION 288197 manufactured by Hycor Biomedical.
[90283522]
The customer stated the lack of instructions resulted in an incorrect interpretation by medical staff where the probe cleaning solution was discarded in an empty distilled water bottle. The water bottle was not properly re- labeled to show it no longer contained di water, but instead the cleaning solution. Another nurse mistakenly used the bottle to mix an oral medication for an eight- year-old patient thinking it was di water. Approximately 1ml of probe cleaning solution was ingested by the patient. The patient's family was notified about the accidental exposure. The patient expressed nausea, oral irritation/bad taste, dizziness, and didn't feel well. As a result, the patient remained in the medical office for an hour for monitoring. While the patient was being monitored, the medical staff discovered that the bottle labeled as di water actually contained cleaning solution and not di water. The patient was discharged uneventfully. The customer was unable to provide further information and/or event details, except that the child did not incur any serious injury as a result of not feeling well (internal reference (b)(4)). Although there was no serious injury as a result of this event, hycor opted to file an mdr conservatively as a result of the patient being monitored due to dizziness, and nausea for an hour. Hycor's medical monitor indicated a remote potential for patient harm exists when instructions provided by hycor are not followed, the reported information was vague and did not provide any specific details indicating how the labeling malfunctioned related to probe cleaning solution disposal instructions. Several follow-up attempts were made to gather further details from dr. (b)(6) but he was unable to provide any further details about this incident, since it had occurred 4 months prior to him reporting this incident to hycor. Hycor performed a labeling review and found that the existing labeling was adequate. No other complaint reports alleging inadequate instructions related to the probe solution disposal were found.
Patient Sequence No: 1, Text Type: N, H10
[90283523]
The customer reported a potential issue with the hytec di (directional insert). The alleged issue indicated the di "does not provide clear instructions for collecting the cleaning solution or provide a container. " hycor opted to report this event conservatively on basis of potential for harm.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2016473-2017-00002 |
| MDR Report Key | 6978069 |
| Date Received | 2017-10-25 |
| Date of Report | 2017-10-25 |
| Date of Event | 2016-11-01 |
| Date Mfgr Received | 2017-03-31 |
| Date Added to Maude | 2017-10-25 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. TARA VIVIANI |
| Manufacturer Street | 7272 CHAPMAN AVE |
| Manufacturer City | GARDEN GROVE CA 92841 |
| Manufacturer Country | US |
| Manufacturer Postal | 92841 |
| Manufacturer Phone | 7149333027 |
| Manufacturer G1 | HYCOR BIOMEDICAL |
| Manufacturer Street | 7272 CHAPMAN AVE |
| Manufacturer City | GARDEN GROVE CA 92841 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 92841 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | HYTEC 288 PROBE CLEANING SOLUTION |
| Generic Name | PROBE CLEANING SOLUTION |
| Product Code | DHB |
| Date Received | 2017-10-25 |
| Catalog Number | 288197 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | HYCOR BIOMEDICAL |
| Manufacturer Address | 7272 CHAPMAN AVE GARDEN GROVE CA 92841 US 92841 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-10-25 |