MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-11 for SPECIFIC/TOTAL IGE EIA 74155 manufactured by Hycor Biomedical.
[114148453]
The distributor reported the shipment containing stop solution (1n sodium hydroxide) was received with a stained carton, suggesting leakage of an item in the package. Photographic evidence provided by the distributor showed two stained cartons. Pictures of the stop solution bottles showed that one bottle had a visibly lower volume than the bottle from the other carton. Hycor requested products be returned for investigation. The investigation demonstrated one of the two returned bottles was leaking as determined by a vacuum test. Further investigation determined that the stop solution bottles used in the kit lot were manufactured during a time when the automatic capping system malfunctioned leading to a temporary process to hand tighten the caps. A stop ship order for product containing stop solution bottles manufactured during the time period when the capping system was not functioning correctly was initiated 05/31/2018. All impacted bottles of stop solution have been reprocessed ensuring that the cap is sealed with the proper torque. A sampling of product was tested in a vacuum chamber to determine if leaking was present, no leaks were detected. Hycor is initiating a recall action to inform distributors that leaking stop solution bottles have been reported during transit and that they should inspect remaining inventory for evidence of leakage prior to further distribution. There were no adverse outcomes reported to hycor. However, out of an abundance of caution, we are filing an mdr. Delay in reporting was due to an employee confusing this event with a previously reported similar event, review of records determined that this event should also have been reported. [(b)(4)].
Patient Sequence No: 1, Text Type: N, H10
[114148454]
The distributor reported the shipment containing stop solution (1n sodium hydroxide) was received with a stained carton, suggesting leakage of an item in the package. Photographic evidence provided by the distributor showed two stained cartons. One carton was stained on the bottom panel, the second carton was stained on the top panel indicating that a bottle from one carton likely leaked and stained the lower carton. Pictures of the stop solution bottles showed that one bottle had a visibly lower volume than the bottle from the other carton. (the container is filled to 300 ml in a 500 ml bottle). Hycor requested products be returned for investigation. Hycor received the damaged products on 06/01/2018. The investigation demonstrated one of the two returned bottles was leaking as determined by a vacuum test. There were no adverse outcomes reported to hycor. However, out of an abundance of caution, we are filing an mdr.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2016473-2018-00002 |
| MDR Report Key | 7679461 |
| Date Received | 2018-07-11 |
| Date of Report | 2018-07-11 |
| Date of Event | 2018-02-19 |
| Date Mfgr Received | 2018-02-19 |
| Device Manufacturer Date | 2017-08-09 |
| Date Added to Maude | 2018-07-11 |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | SPECIFIC/TOTAL IGE EIA |
| Generic Name | SPECIFIC/TOTAL IGE EIA |
| Product Code | DHB |
| Date Received | 2018-07-11 |
| Returned To Mfg | 2018-06-01 |
| Catalog Number | 74155 |
| Lot Number | 154104-9 |
| Device Expiration Date | 2018-11-30 |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| 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 | 2018-07-11 |