FDA Device recall Z-0886-2013
Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290)
- FDA Device
- Class II
- terminated
- Published 2013-03-06
On 2013-03-06 the FDA classified a Class II recall of Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290) by Integra Lifesciences, citing addendum to the Instructions for Use. The addendum emphasizes the warnings and precautions already contained in the device's IFU and also provides additional warnings and precauti….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0886-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-12 |
| Published | 2013-03-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Integra Lifesciences |
| Distribution | US |
Product
Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in endoscopic surgery. For use when a rigid endoscopic instrument for grasping and/or dissecting if soft tissue is determined to be appropriate by the surgeon. Monopolar electrosurgical current can be used for coagulation and/or cutting.
Reason
Addendum to the Instructions for Use. The addendum emphasizes the warnings and precautions already contained in the device's IFU and also provides additional warnings and precautions that are applicable to the use of electrosurgical equipment in health care facility environments.
Identifiers
| code_info | Catalogue No. 600-290. All lots distributed since 2004. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0886-2013%22
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