PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for… — Class II medical device recall Z-0960-2019
Terminated recall by Abbott Vascular, reported 2019-03-06, distributed nationwide. Incorrect expiration being entered for one lot.
| Recall number | Z-0960-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abbott Vascular, Temecula, CA, United States |
| Recall initiated | 2018-07-03 |
| Classified | 2019-02-26 |
| Reported by FDA | 2019-03-06 |
| Distributed | Nationwide (US) |
| Quantity | 26 units |
| Reason classes | labeling |
| Lot numbers | 60047593 |
| Model numbers | 1000185 |
Product
PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).
Reason for recall
Incorrect expiration being entered for one lot.
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-0960-2019. 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.