MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-08 for ISPAN PERFLUOROPROPANE (C3F8) GAS 8065797105 manufactured by Air Liquide.
[116732974]
No sample has been received by manufacturing for evaluation. Investigation including root cause analysis is in progress. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when additional reportable information becomes available. Additional information has been requested. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[116732975]
A nurse reported that ophthalmic gas was instilled into a patient's eye during surgery. The gas bubble lasted only a short duration and did not hold the retina against the choroid. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1610287-2018-00032 |
MDR Report Key | 7761358 |
Date Received | 2018-08-08 |
Date of Report | 2018-10-19 |
Date of Event | 2018-07-24 |
Date Mfgr Received | 2018-10-09 |
Device Manufacturer Date | 2017-08-09 |
Date Added to Maude | 2018-08-08 |
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 | MR. BRYAN BLAKE |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8176152230 |
Manufacturer G1 | AIR LIQUIDE |
Manufacturer Street | 13140 TI BLVD. |
Manufacturer City | DALLAS TX 75243 |
Manufacturer Country | US |
Manufacturer Postal Code | 75243 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 0 |
Brand Name | ISPAN PERFLUOROPROPANE (C3F8) GAS |
Generic Name | INTRAOCULAR GAS |
Product Code | LPO |
Date Received | 2018-08-08 |
Model Number | NA |
Catalog Number | 8065797105 |
Lot Number | 722119 |
Device Expiration Date | 2019-07-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | AIR LIQUIDE |
Manufacturer Address | 13140 TI BLVD. DALLAS TX 75243 US 75243 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2018-08-08 |