MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-23 for CADENCE PHYSIO PRECONNECT 22550PC manufactured by Covidien.
[187558303]
The incident sample has been requested but to date has not been received for evaluation. If the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted.? As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.
Patient Sequence No: 1, Text Type: N, H10
[187558304]
The customer reported that when the plastic backing is peeled off of the pad, the gel is pulling off onto the plastic backing.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1219103-2020-00277 |
MDR Report Key | 9867041 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-23 |
Date of Report | 2020-03-23 |
Date Mfgr Received | 2020-03-11 |
Date Added to Maude | 2020-03-23 |
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 | JILL SARAIVA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5086183640 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | 2 LUDLOW PARKWAY |
Manufacturer City | CHICOPEE MA 01022 |
Manufacturer Country | US |
Manufacturer Postal Code | 01022 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CADENCE PHYSIO PRECONNECT |
Generic Name | PACEMAKER, CARDIAC, EXTERNAL TRANSCUTANEOUS (NON-INVASIVE) |
Product Code | DRO |
Date Received | 2020-03-23 |
Model Number | 22550PC |
Catalog Number | 22550PC |
Lot Number | 912034X |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | 2 LUDLOW PARKWAY CHICOPEE MA 01022 US 01022 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-23 |