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Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2421-2024 — CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 (21-2120, 21-2125, and 21-2127) Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a contin

U.S. FDA — Device Enforcement · United States · 2024-02-27 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2421-2024
Date of alert: 2024-02-27
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Smiths Medical ASD Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10610586040429

Reported risk: The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidural space, or subarachnoid space infusion.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.