DeviceSignal · Recall classified

TISSIUM SA

FDA classified a device recall on 2026-08-06 · Class II · Z-2902-2026

EventRecall classified
Effective2026-08-06
ClassificationClass II

On 2026-08-06 the FDA classified a device recall from TISSIUM SA as Class II. Product: Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number…. Recall Z-2902-2026. The firm initiated it on 2026-06-15. This reports the classification FDA published on that date.

Reported facts

Recall number
Z-2902-2026
Classification
Class II
Classified on
2026-08-06
Initiated on
2026-06-15
Firm
TISSIUM SA
Reason
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may result in perioperative breakage of the device rendering device unusable; worst-case outcome would be revision surgery.
Product
Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO1575 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No

Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.

Provenance

Source
fda_device_enforcement
Source record
Z-2902-2026
Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72
Source URL
https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
Observed
2026-09-08T16:22:09.483Z
Transform
fda_device_enforcement_to_recall v1
Event rule
fda_device_recall_classified v1
Event key
e069cbd586d5eba939382efc9089f4e3d04c81f078e24efb73479739449b3347
Signal type
device_recall.classified

Source terms that apply

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Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)