MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2008-12-12 for OFFSET SWIVAL CLAMP BAR & TRAPEZE, HEAVY DUTY 00-0640-021 manufactured by Zimmer Orthopaedic Surgical Products.
[1034096]
Clamps broke during use.
Patient Sequence No: 1, Text Type: D, B5
[8162797]
Additional catalog #: 00-0640-003.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1035617-2008-00015 |
MDR Report Key | 1310024 |
Report Source | 05 |
Date Received | 2008-12-12 |
Date of Report | 2008-11-14 |
Date of Event | 2008-11-10 |
Date Mfgr Received | 2008-11-14 |
Date Added to Maude | 2010-04-26 |
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 | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | JOHN WATKINS |
Manufacturer Street | 200 WEST OHIO AVENUE |
Manufacturer City | DOVER OH 44622 |
Manufacturer Country | US |
Manufacturer Postal | 44622 |
Manufacturer Phone | 3303649483 |
Manufacturer G1 | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS |
Manufacturer Street | 2021 OLD MOUNTAIN ROAD |
Manufacturer City | STATESVILLE NC 28677 |
Manufacturer Country | US |
Manufacturer Postal Code | 28677 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OFFSET SWIVAL CLAMP BAR & TRAPEZE, HEAVY DUTY |
Generic Name | CLAMP BAR & TRAPEZE |
Product Code | ILZ |
Date Received | 2008-12-12 |
Catalog Number | 00-0640-021 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS |
Manufacturer Address | STATESVILLE NC US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2008-12-12 |