Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The… — Class III medical device recall Z-1198-2019
Terminated recall by Cordis Corporation, reported 2019-04-24, distributed nationwide. Frayed pieces of the mounting card being inside the primary packaging.
| Recall number | Z-1198-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis Corporation, Miami Lakes, FL, United States |
| Recall initiated | 2019-02-07 |
| Classified | 2019-04-18 |
| Reported by FDA | 2019-04-24 |
| Terminated | 2021-11-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, SG |
| Quantity | 23,481 |
| Lot numbers | 17722359, 17722360, 17724480, 17724819, 17729208, 17733005, 17733016, 17733019, 17735189, 17735533, 17735534, 17736643, 17737608, 17740605, 17740611, 17742559, 17742581, 17743099, 17743101, 17744429, 17744430, 17744955, 17745965, 17746022, 17746026, 17746147, 17747583, 17747584, 17748743, 17749793, 17749800, 17750476, 17750494, 17750783, 17750785, 17752698, 17752703, 17753002, 17753948, 17753959 and 133 more |
Product
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
Reason for recall
Frayed pieces of the mounting card being inside the primary packaging.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1198-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.