Class I — IMPERATIVE CARE INC
| Recalling firm | Imperative Care Inc. |
|---|---|
| Registered facility | IMPERATIVE CARE INC. (the firm's only registered facility) |
| Classification | Class I |
| Status | Completed |
| Reason | There is a potential for distal end of catheters to fracture and become detached. |
| Product | Imperative Care, ZOOM 71 Reperfusion Catheter, REF: ICRC071137, TRX Tip, 137 cm, 6F (.083 in/2.11 mm), .071 in/1.8 mm), STERILE.EO, Rx Only, UDI: (01) 00812212030191. For neurovascular procedures. |
| Quantity | 3118 units |
| Distribution | US nationwide distribution. |
| Initiated | 2021-08-13 |
| Classified | 2021-09-29 |
| Recall number | Z-2577-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — IMPERATIVE CARE INC (Z-2577-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88611/
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