MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-18 for LF1737 LF1737RR manufactured by Stryker Sustainability Solutions Lakeland.
Report Number | 0001056128-2020-00015 |
MDR Report Key | 9851139 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-18 |
Date of Report | 2020-03-18 |
Date of Event | 2020-01-21 |
Date Mfgr Received | 2020-02-19 |
Device Manufacturer Date | 2019-10-24 |
Date Added to Maude | 2020-03-18 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. MARISSA RICHMOND |
Manufacturer Street | 1810 W. DRAKE DRIVE |
Manufacturer City | TEMPE AZ 85283 |
Manufacturer Country | US |
Manufacturer Postal | 85283 |
Manufacturer Phone | 8888883433 |
Manufacturer G1 | STRYKER SUSTAINABILITY SOLUTIONS LAKELAND |
Manufacturer Street | 5300 REGION CT |
Manufacturer City | LAKELAND FL 33815 |
Manufacturer Country | US |
Manufacturer Postal Code | 33815 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NA |
Generic Name | ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, R |
Product Code | NUJ |
Date Received | 2020-03-18 |
Returned To Mfg | 2020-01-30 |
Model Number | LF1737 |
Catalog Number | LF1737RR |
Lot Number | 11075578 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER SUSTAINABILITY SOLUTIONS LAKELAND |
Manufacturer Address | 5300 REGION CT LAKELAND FL 33815 US 33815 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-18 |