MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2000-01-21 for STERI-GAS 4-100 CARTRIDGE manufactured by 3m Co..
[162206]
A health care worker opened the door of the sterilizer and had a hard time getting the cartridge out. Worker saw liquid in the sterilizer and some liquid spilled on her.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2110898-2000-00003 |
MDR Report Key | 259935 |
Report Source | 05,07 |
Date Received | 2000-01-21 |
Date of Report | 2000-01-12 |
Date of Event | 1999-12-07 |
Date Mfgr Received | 1999-12-07 |
Date Added to Maude | 2000-01-28 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | GAIL STEWARD |
Manufacturer Street | 3M CENTER BLDG., 275-3E-08 PO BOX 33275 |
Manufacturer City | ST. PAUL MN 551333275 |
Manufacturer Country | US |
Manufacturer Postal | 551333275 |
Manufacturer Phone | 6127369057 |
Manufacturer G1 | 3M |
Manufacturer Street | 1617 N. FRONT ST. P.O. BOX 95 |
Manufacturer City | NEW ULM MN 56073009 |
Manufacturer Country | US |
Manufacturer Postal Code | 56073 0095 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | STERI-GAS 4-100 CARTRIDGE |
Generic Name | EO GAS CARTRIDGE |
Product Code | FLI |
Date Received | 2000-01-21 |
Model Number | NA |
Catalog Number | 4-100 |
Lot Number | UNK |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 251735 |
Manufacturer | 3M CO. |
Manufacturer Address | 3M CENTER, BLDG. 275-3E-08 PO BOX 33275 ST. PAUL MN 551333275 US |
Baseline Brand Name | STERI-GAS |
Baseline Generic Name | EO GAS CATRIDGE |
Baseline Model No | NA |
Baseline Catalog No | 4-100 |
Baseline ID | * |
Baseline Device Family | STERILIZATION HARDWARE |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2000-01-21 |