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

Recall Z-2362-2015 — Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

U.S. FDA — Device Enforcement · United States · 2015-07-21 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2362-2015
Date of alert: 2015-07-21
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: CareFusion 303, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 49000226

Reported risk: Channel Error code is displayed on the PC unit with an audio and visual alarm, and on the syringe module. After the error is cleared on the PCU, the syringe pump is unresponsive to key presses until the next power cycle, or the module is detached and reattached.

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

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Recall Z-2362-2015 — Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

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